Human (GRCh37.p13)
Description

amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 12 [Source:HGNC Symbol;Acc:14439]

About this transcript

This transcript has 15 exons, is annotated with 9 domains and features, is associated with 27465 variant alleles and maps to 565 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000405148.2ALS2CR12-2012013445aaENSP00000385098.2
 
Protein coding
CCDS2346C9JTY0 Q96Q35 NM_139163.2GENCODE basic
ENST00000392257.3ALS2CR12-0021943422aaENSP00000376086.3
 
Protein coding
CCDS46488C9JTY0 Q96Q35 NM_001127391.1GENCODE basic
ENST00000286190.5ALS2CR12-0011769445aaENSP00000286190.5
 
Protein coding
CCDS2346C9JTY0 Q96Q35 -GENCODE basic
ENST00000439709.1ALS2CR12-0041626422aaENSP00000412073.1
 
Protein coding
CCDS46488C9JTY0 Q96Q35 -GENCODE basic
ENST00000415745.1ALS2CR12-008782124aaENSP00000402327.1
 
Protein coding
--CDS 5' incomplete
ENST00000418364.1ALS2CR12-00945849aaENSP00000407585.1
 
Protein coding
C9JTY0 -CDS 3' incomplete
ENST00000425488.1ALS2CR12-005430143aaENSP00000393945.1
 
Protein coding
C9JZS0 -CDS 3' incomplete
ENST00000448967.1ALS2CR12-006721No protein-
 
Processed transcript
---
ENST00000494171.1ALS2CR12-0032075No protein-
 
Retained intron
---
ENST00000494223.1ALS2CR12-007394No protein-
 
Retained intron
---
Statistics

Exons: 15, Coding exons: 14, Transcript length: 1,943 bps, Translation length: 422 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96Q35

CCDS

This transcript is a member of the Human CCDS set: CCDS46488

Version

ENST00000392257.3

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000256287 (version 2)
GENCODE basic gene

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