Canonical Allele Identifier: CA1327820270

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216412665C= , CM000664.2:g.216412665C=	GRCh38
NC_000002.11:g.217277388C= , CM000664.1:g.217277388C=	GRCh37
NC_000002.10:g.216985633C=	NCBI36
NG_009771.1:g.5252C= , LRG_108:g.5252C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425815.6:c.-148C=	ENSP00000394410.2:n.-148C=
ENST00000430374.6:c.-96+62C=	ENSP00000405077.2:n.-96+62C=
ENST00000444508.6:c.-165C=	ENSP00000398969.2:n.-165C=
ENST00000697898.1:n.266+17C=
ENST00000697899.1:c.-96+17C=	ENSP00000513470.1:n.-96+17C=
ENST00000697900.1:n.181+17C=
ENST00000697901.1:c.-96+17C=	ENSP00000513471.1:n.-96+17C=
ENST00000697902.1:n.137+17C=
ENST00000697903.1:c.-96+17C=	ENSP00000513472.1:n.-96+17C=
ENST00000357276.9:c.-96+17C= MANE Select	ENSP00000349823.4:n.-96+17C=
ENST00000357276.8:c.-96+17C=	ENSP00000349823.4:n.-96+17C=
ENST00000425815.5:c.-148C=	ENSP00000394410.1:n.-148C=
ENST00000430374.5:c.-96+62C=	ENSP00000405077.1:n.-96+62C=
ENST00000444508.5:c.-165C=	ENSP00000398969.1:n.-165C=
NM_014140.3:c.-96+17C= , LRG_108t1:c.-96+17C=	NP_054859.2:n.-96+17C=
XM_005246631.2:c.-96+62C=	XP_005246688.1:n.-96+62C=
XM_005246632.1:c.-165C=	XP_005246689.1:n.-165C=
XM_006712557.1:c.-96+17C=	XP_006712620.1:n.-96+17C=
XM_005246632.2:c.-165C=	XP_005246689.1:n.-165C=
NM_014140.4:c.-96+17C= MANE Select	NP_054859.2:n.-96+17C=