Human (GRCh38.p14)
Description

SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 1 [Source:HGNC Symbol;Acc:HGNC:11104]

Gene Synonyms

BAF155, CRACC1, RSC8, SRG3

Location

Chromosome 3: 47,585,269-47,782,106 reverse strand.

GRCh38:CM000665.2

About this gene

This gene has 8 transcripts (splice variants), 231 orthologues, 3 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000254480.10SMARCC1-20163541105aaENSP00000254480.5
 
Protein coding
CCDS2758Q92922 NM_003074.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000454240.1SMARCC1-203636133aaENSP00000414266.1
 
Nonsense mediated decay
F8WE13 -TSL:3
ENST00000425518.5SMARCC1-2023827No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000462198.5SMARCC1-204785No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000492896.1SMARCC1-208568No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000485833.1SMARCC1-207412No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000483847.1SMARCC1-205804No protein-
 
Retained intron
--TSL:2
ENST00000485737.1SMARCC1-206631No protein-
 
Retained intron
--TSL:4