Canonical Allele Identifier: CA1327821541

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216415486T= , CM000664.2:g.216415486T=	GRCh38
NC_000002.11:g.217280209T= , CM000664.1:g.217280209T=	GRCh37
NC_000002.10:g.216988454T=	NCBI36
NG_009771.1:g.8073T= , LRG_108:g.8073T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.782T=	ENSP00000394410.2:p.Val261=
ENST00000430374.6:c.782T=	ENSP00000405077.2:p.Val261=
ENST00000444508.6:c.782T=	ENSP00000398969.2:p.Val261=
ENST00000697898.1:n.1143T=
ENST00000697899.1:c.782T=	ENSP00000513470.1:p.Val261=
ENST00000697900.1:n.1058T=
ENST00000697901.1:c.782T=	ENSP00000513471.1:p.Val261=
ENST00000697902.1:n.1014T=
ENST00000697903.1:c.782T=	ENSP00000513472.1:p.Val261=
ENST00000697904.1:c.782T=	ENSP00000513473.1:p.Val261=
ENST00000697905.1:c.782T=	ENSP00000513474.1:p.Val261=
ENST00000697906.1:c.782T=	ENSP00000513475.1:p.Val261=
ENST00000697907.1:c.782T=	ENSP00000513476.1:p.Val261=
ENST00000357276.9:c.782T= MANE Select	ENSP00000349823.4:p.Val261=
ENST00000357276.8:c.782T=	ENSP00000349823.4:p.Val261=
ENST00000358207.9:c.782T=	ENSP00000350940.5:p.Val261=
ENST00000392128.6:c.374T=	ENSP00000375974.2:p.Val125=
ENST00000427645.5:c.479T=	ENSP00000392997.1:p.Val160=
NM_001127207.1:c.782T=	NP_001120679.1:p.Val261=
NM_014140.3:c.782T= , LRG_108t1:c.782T=	NP_054859.2:p.Val261=
XM_005246631.2:c.782T=	XP_005246688.1:p.Val261=
XM_005246632.1:c.782T=	XP_005246689.1:p.Val261=
XM_006712557.1:c.782T=	XP_006712620.1:p.Val261=
XM_005246632.2:c.782T=	XP_005246689.1:p.Val261=
XM_017004228.2:c.-135T=	XP_016859717.1:n.-135T=
NM_001127207.2:c.782T=	NP_001120679.1:p.Val261=
NM_014140.4:c.782T= MANE Select	NP_054859.2:p.Val261=