Human (GRCh38.p14)
Description

ALS2 C-terminal like [Source:HGNC Symbol;Acc:HGNC:20605]

Gene Synonyms

DKFZP686I0110, FLJ36525, RN49018

Location

Chromosome 3: 46,668,995-46,693,704 reverse strand.

GRCh38:CM000665.2

About this gene

This gene has 10 transcripts (splice variants), 130 orthologues and 7 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000318962.9ALS2CL-2014913953aaENSP00000313670.4
 
Protein coding
CCDS2743Q60I27-1 NM_147129.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000415953.5ALS2CL-2033471953aaENSP00000413223.1
 
Protein coding
CCDS2743Q60I27-1 -GENCODE basicAPPRIS P1TSL:2
ENST00000423707.5ALS2CL-2044470302aaENSP00000395749.1
 
Nonsense mediated decay
H7C0M4 -TSL:2CDS 5' incomplete
ENST00000434140.5ALS2CL-2063937535aaENSP00000405335.1
 
Nonsense mediated decay
G5E9N5 -TSL:1
ENST00000383742.7ALS2CL-2021747No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000473484.1ALS2CL-208564No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000450172.5ALS2CL-2076593No protein-
 
Retained intron
--TSL:2
ENST00000431015.5ALS2CL-2056563No protein-
 
Retained intron
--TSL:2
ENST00000486301.5ALS2CL-2094431No protein-
 
Retained intron
--TSL:5
ENST00000498817.5ALS2CL-2101065No protein-
 
Retained intron
--TSL:3