Human (GRCh37.p13)
Description

complement component 1, r subcomponent [Source:HGNC Symbol;Acc:1246]

Location
About this transcript

This transcript has 11 exons, is annotated with 37 domains and features, is associated with 3592 variant alleles and maps to 510 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000542285.1C1R-2012112653aaENSP00000438615.1
 
Protein coding
F5GWL0 F5H1N6 F5H3A3
H0YFH3
-GENCODE basic
ENST00000542220.2C1R-0011257346aaENSP00000438682.2
 
Protein coding
F5GWL0 F5H1N6 F5H3A3
F6T9X8
NM_001733.4CDS 3' incomplete
ENST00000602480.1C1R-0021168281aaENSP00000474998.1
 
Protein coding
-NM_001733.4CDS 5' incomplete
ENST00000536053.2C1R-0031156360aaENSP00000444271.2
 
Protein coding
B4DPQ0 F5GWL0 F5GZR1
F5H1N6 F5H3A3
-CDS 3' incomplete
ENST00000535233.2C1R-0041020312aaENSP00000438636.2
 
Protein coding
F5H2D0 -CDS 3' incomplete
ENST00000602286.1C1R-005956281aaENSP00000473278.1
 
Protein coding
--CDS 5' incomplete
ENST00000541042.1C1R-00759171aaENSP00000441601.1
 
Protein coding
F5GWL0 F5H1N6 -CDS 3' incomplete
ENST00000540242.1C1R-008575156aaENSP00000442946.1
 
Protein coding
F5H6Y3 -CDS 3' incomplete
ENST00000538050.1C1R-00955349aaENSP00000444009.1
 
Protein coding
F5H1N6 -CDS 3' incomplete
ENST00000543835.1C1R-010521156aaENSP00000445285.1
 
Protein coding
F5GWL0 F5H1N6 F5H3N3
-CDS 3' incomplete
ENST00000540610.1C1R-01151993aaENSP00000439223.1
 
Protein coding
F5GWL0 F5H1N6 F5H3A3
-CDS 3' incomplete
ENST00000543362.1C1R-006832144aaENSP00000446356.1
 
Nonsense mediated decay
F5H1V0 --
ENST00000602298.1C1R-015564No protein-
 
Processed transcript
---
ENST00000540394.2C1R-0122103No protein-
 
Retained intron
---
ENST00000536092.1C1R-013632No protein-
 
Retained intron
---
ENST00000545466.1C1R-014597No protein-
 
Retained intron
---
ENST00000543851.1C1R-016476No protein-
 
Retained intron
---
Statistics

Exons: 11, Coding exons: 10, Transcript length: 2,112 bps, Translation length: 653 residues

Version

ENST00000542285.1

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.

Stop codons

This transcript has a variant, rs1126605, that causes a stop codon to be gained in at least 10% of HapMap or 1000 Genome population(s) CSHL-HAPMAP:HAPMAP-LWK, CSHL-HAPMAP:HAPMAP-TSI, CSHL-HAPMAP:HapMap-YRI, CSHL-HAPMAP:HAPMAP-CHB, CSHL-HAPMAP:HapMap-JPT, CSHL-HAPMAP:HapMap-HCB, CSHL-HAPMAP:HAPMAP-CHD, CSHL-HAPMAP:HAPMAP-GIH.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.