Canonical Allele Identifier: CA1327820202

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216412507A= , CM000664.2:g.216412507A=	GRCh38
NC_000002.11:g.217277230A= , CM000664.1:g.217277230A=	GRCh37
NC_000002.10:g.216985475A=	NCBI36
NG_009771.1:g.5094A= , LRG_108:g.5094A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000430374.6:c.-192A=	ENSP00000405077.2:n.-192A=
ENST00000697898.1:n.125A=
ENST00000697899.1:c.-237A=	ENSP00000513470.1:n.-237A=
ENST00000697900.1:n.40A=
ENST00000357276.9:c.-237A= MANE Select	ENSP00000349823.4:n.-237A=
ENST00000357276.8:c.-237A=	ENSP00000349823.4:n.-237A=
ENST00000430374.5:c.-192A=	ENSP00000405077.1:n.-192A=
NM_014140.3:c.-237A= , LRG_108t1:c.-237A=	NP_054859.2:n.-237A=
XM_005246631.2:c.-192A=	XP_005246688.1:n.-192A=
XM_006712557.1:c.-237A=	XP_006712620.1:n.-237A=
NM_014140.4:c.-237A= MANE Select	NP_054859.2:n.-237A=