Human (GRCh38.p14)
Description

SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 [Source:HGNC Symbol;Acc:HGNC:18398]

Gene Synonyms

DKFZP762K2015, ETL1, KIAA1122

Location

Chromosome 4: 94,207,611-94,291,292 forward strand.

GRCh38:CM000666.2

About this gene

This gene has 8 transcripts (splice variants), 226 orthologues, 30 paralogues and is associated with 6 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000354268.9SMARCAD1-20150941026aaENSP00000346217.4
 
Protein coding
CCDS3639Q9H4L7-1 NM_020159.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000359052.8SMARCAD1-20250171028aaENSP00000351947.4
 
Protein coding
CCDS47101Q9H4L7-2 -APPRIS ALT1TSL:1
ENST00000457823.6SMARCAD1-20446491028aaENSP00000415576.2
 
Protein coding
CCDS47101Q9H4L7-2 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000509418.1SMARCAD1-2062348596aaENSP00000423286.1
 
Protein coding
CCDS58914Q9H4L7-3 -GENCODE basicTSL:2
ENST00000394961.6SMARCAD1-203377870aaENSP00000378413.2
 
Nonsense mediated decay
F8W9M2 -TSL:2
ENST00000510105.5SMARCAD1-2072409244aaENSP00000424624.1
 
Nonsense mediated decay
D6RAY8 -TSL:5
ENST00000506089.1SMARCAD1-205554No protein-
 
Retained intron
--TSL:4
ENST00000514232.1SMARCAD1-208444No protein-
 
Retained intron
--TSL:3