Canonical Allele Identifier: CA1327820206

Gene: SMARCAL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216412521A= , CM000664.2:g.216412521A=	GRCh38
NC_000002.11:g.217277244A= , CM000664.1:g.217277244A=	GRCh37
NC_000002.10:g.216985489A=	NCBI36
NG_009771.1:g.5108A= , LRG_108:g.5108A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000430374.6:c.-178A=	ENSP00000405077.2:n.-178A=
ENST00000444508.6:c.-309A=	ENSP00000398969.2:n.-309A=
ENST00000697898.1:n.139A=
ENST00000697899.1:c.-223A=	ENSP00000513470.1:n.-223A=
ENST00000697900.1:n.54A=
ENST00000697901.1:c.-223A=	ENSP00000513471.1:n.-223A=
ENST00000697902.1:n.10A=
ENST00000697903.1:c.-223A=	ENSP00000513472.1:n.-223A=
ENST00000357276.9:c.-223A= MANE Select	ENSP00000349823.4:n.-223A=
ENST00000357276.8:c.-223A=	ENSP00000349823.4:n.-223A=
ENST00000430374.5:c.-178A=	ENSP00000405077.1:n.-178A=
ENST00000444508.5:c.-309A=	ENSP00000398969.1:n.-309A=
NM_014140.3:c.-223A= , LRG_108t1:c.-223A=	NP_054859.2:n.-223A=
XM_005246631.2:c.-178A=	XP_005246688.1:n.-178A=
XM_005246632.1:c.-309A=	XP_005246689.1:n.-309A=
XM_006712557.1:c.-223A=	XP_006712620.1:n.-223A=
NM_014140.4:c.-223A= MANE Select	NP_054859.2:n.-223A=