Canonical Allele Identifier: CA1677059338

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437209A= , CM000668.2:g.160437209A=	GRCh38
NC_000006.11:g.160858241A= , CM000668.1:g.160858241A=	GRCh37
NC_000006.10:g.160778231A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1286A= MANE Select	ENSP00000275300.2:p.Glu429=
ENST00000275300.2:c.1286A=	ENSP00000275300.2:p.Glu429=
NM_021977.3:c.1286A=	NP_068812.1:p.Glu429=
XM_005267106.3:c.893A=	XP_005267163.1:p.Glu298=
XM_011536075.1:c.830A=	XP_011534377.1:p.Glu277=
XM_011536076.1:c.830A=	XP_011534378.1:p.Glu277=
XM_011536077.1:c.830A=	XP_011534379.1:p.Glu277=
XR_245546.1:n.1018-5552A=
XM_005267106.5:c.893A=	XP_005267163.1:p.Glu298=
XM_011536075.2:c.830A=	XP_011534377.1:p.Glu277=
XM_011536076.3:c.830A=	XP_011534378.1:p.Glu277=
XM_017011203.2:c.830A=	XP_016866692.1:p.Glu277=
XR_001743588.1:n.1230A=
XR_001743589.1:n.1018-5552A=
NM_021977.4:c.1286A= MANE Select	NP_068812.1:p.Glu429=