Human (GRCh38.p14)
Description

transgelin [Source:HGNC Symbol;Acc:HGNC:11553]

Gene Synonyms

DKFZP686P11128, SM22, SMCC, TAGLN1, WS3-10

Location

Chromosome 11: 117,199,370-117,207,464 forward strand.

GRCh38:CM000673.2

About this gene

This gene has 8 transcripts (splice variants), 287 orthologues and 5 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000392951.9TAGLN-2023786201aaENSP00000376678.4
 
Protein coding
CCDS8381Q01995 Q5U0D2 NM_003186.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000532870.5TAGLN-2072166201aaENSP00000432282.1
 
Protein coding
CCDS8381Q01995 Q5U0D2 -GENCODE basicAPPRIS P1TSL:1
ENST00000278968.10TAGLN-2011477201aaENSP00000278968.6
 
Protein coding
CCDS8381Q01995 Q5U0D2 -APPRIS P1TSL:1
ENST00000530649.5TAGLN-2061227201aaENSP00000431941.1
 
Protein coding
CCDS8381Q01995 Q5U0D2 -GENCODE basicAPPRIS P1TSL:1
ENST00000525531.5TAGLN-2031048201aaENSP00000432054.1
 
Protein coding
CCDS8381Q01995 Q5U0D2 -APPRIS P1TSL:5
ENST00000529622.1TAGLN-204501151aaENSP00000432380.1
 
Protein coding
H0YCU9 -TSL:3CDS 5' incomplete
ENST00000529792.5TAGLN-20537591aaENSP00000431862.1
 
Protein coding
E9PJ32 -TSL:3CDS 3' incomplete
ENST00000533863.1TAGLN-2083298No protein-
 
Retained intron
--TSL:1