Human (GRCh37.p13)
Description

CHURC1-FNTB readthrough [Source:HGNC Symbol;Acc:42960]

Location
About this transcript

This transcript has 14 exons, is annotated with 9 domains and features, is associated with 63991 variant alleles and maps to 503 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000549987.1CHURC1-FNTB-0011468472aaENSP00000447121.1
 
Protein coding
B3KSC2 B4DJ86 B4DL54
H0YHI0
NM_001202559.1Ensembl CanonicalGENCODE BasicCDS 5' incomplete
ENST00000553743.1CHURC1-FNTB-00420769aaENSP00000450692.1
 
Protein coding
H0YJ25 -CDS 5' and 3' incomplete
ENST00000552941.1CHURC1-FNTB-0021847107aaENSP00000449668.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000551823.1CHURC1-FNTB-00351785aaENSP00000449709.1
 
Nonsense mediated decay
H0YIM9 -CDS 5' incomplete
Statistics

Exons: 14, Coding exons: 14, Transcript length: 1,468 bps, Translation length: 472 residues

Incomplete CDS

CDS 5' incomplete

Version

ENST00000549987.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000408068 (version 1)
GENCODE basic gene

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