Canonical Allele Identifier: CA431164458

Gene: SMARCAL1

Linked Data

• gnomAD v4: 2-216412518-C-A
• MyVariant Identifiers: chr2:g.217277241C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216412518C>A , CM000664.2:g.216412518C>A	GRCh38
NC_000002.11:g.217277241C>A , CM000664.1:g.217277241C>A	GRCh37
NC_000002.10:g.216985486C>A	NCBI36
NG_009771.1:g.5105C>A , LRG_108:g.5105C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000430374.6:c.-181C>A	ENSP00000405077.2:n.-181C>A
ENST00000444508.6:c.-312C>A	ENSP00000398969.2:n.-312C>A
ENST00000697898.1:n.136C>A
ENST00000697899.1:c.-226C>A	ENSP00000513470.1:n.-226C>A
ENST00000697900.1:n.51C>A
ENST00000697901.1:c.-226C>A	ENSP00000513471.1:n.-226C>A
ENST00000697902.1:n.7C>A
ENST00000697903.1:c.-226C>A	ENSP00000513472.1:n.-226C>A
ENST00000357276.9:c.-226C>A MANE Select	ENSP00000349823.4:n.-226C>A
ENST00000357276.8:c.-226C>A	ENSP00000349823.4:n.-226C>A
ENST00000430374.5:c.-181C>A	ENSP00000405077.1:n.-181C>A
ENST00000444508.5:c.-312C>A	ENSP00000398969.1:n.-312C>A
NM_014140.3:c.-226C>A , LRG_108t1:c.-226C>A	NP_054859.2:n.-226C>A
XM_005246631.2:c.-181C>A	XP_005246688.1:n.-181C>A
XM_005246632.1:c.-312C>A	XP_005246689.1:n.-312C>A
XM_006712557.1:c.-226C>A	XP_006712620.1:n.-226C>A
NM_014140.4:c.-226C>A MANE Select	NP_054859.2:n.-226C>A