Canonical Allele Identifier: CA431164398

Gene: SMARCAL1

Linked Data

• MyVariant Identifiers: chr2:g.217277232T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216412509T>A , CM000664.2:g.216412509T>A	GRCh38
NC_000002.11:g.217277232T>A , CM000664.1:g.217277232T>A	GRCh37
NC_000002.10:g.216985477T>A	NCBI36
NG_009771.1:g.5096T>A , LRG_108:g.5096T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000430374.6:c.-190T>A	ENSP00000405077.2:n.-190T>A
ENST00000697898.1:n.127T>A
ENST00000697899.1:c.-235T>A	ENSP00000513470.1:n.-235T>A
ENST00000697900.1:n.42T>A
ENST00000357276.9:c.-235T>A MANE Select	ENSP00000349823.4:n.-235T>A
ENST00000357276.8:c.-235T>A	ENSP00000349823.4:n.-235T>A
ENST00000430374.5:c.-190T>A	ENSP00000405077.1:n.-190T>A
NM_014140.3:c.-235T>A , LRG_108t1:c.-235T>A	NP_054859.2:n.-235T>A
XM_005246631.2:c.-190T>A	XP_005246688.1:n.-190T>A
XM_006712557.1:c.-235T>A	XP_006712620.1:n.-235T>A
NM_014140.4:c.-235T>A MANE Select	NP_054859.2:n.-235T>A