Canonical Allele Identifier: CA1677059422

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437380T= , CM000668.2:g.160437380T=	GRCh38
NC_000006.11:g.160858412T= , CM000668.1:g.160858412T=	GRCh37
NC_000006.10:g.160778402T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1288+169T= MANE Select	ENSP00000275300.2:n.1288+169T=
ENST00000275300.2:c.1288+169T=	ENSP00000275300.2:n.1288+169T=
NM_021977.3:c.1288+169T=	NP_068812.1:n.1288+169T=
XM_005267106.3:c.895+169T=	XP_005267163.1:n.895+169T=
XM_011536075.1:c.832+169T=	XP_011534377.1:n.832+169T=
XM_011536076.1:c.832+169T=	XP_011534378.1:n.832+169T=
XM_011536077.1:c.832+169T=	XP_011534379.1:n.832+169T=
XR_245546.1:n.1018-5381T=
XM_005267106.5:c.895+169T=	XP_005267163.1:n.895+169T=
XM_011536075.2:c.832+169T=	XP_011534377.1:n.832+169T=
XM_011536076.3:c.832+169T=	XP_011534378.1:n.832+169T=
XM_017011203.2:c.832+169T=	XP_016866692.1:n.832+169T=
XR_001743588.1:n.1232+169T=
XR_001743589.1:n.1018-5381T=
NM_021977.4:c.1288+169T= MANE Select	NP_068812.1:n.1288+169T=