Canonical Allele Identifier: CA1677059179

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436861A= , CM000668.2:g.160436861A=	GRCh38
NC_000006.11:g.160857893A= , CM000668.1:g.160857893A=	GRCh37
NC_000006.10:g.160777883A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1057A= MANE Select	ENSP00000275300.2:p.Ile353=
ENST00000275300.2:c.1057A=	ENSP00000275300.2:p.Ile353=
NM_021977.3:c.1057A=	NP_068812.1:p.Ile353=
XM_005267106.3:c.664A=	XP_005267163.1:p.Ile222=
XM_011536075.1:c.601A=	XP_011534377.1:p.Ile201=
XM_011536076.1:c.601A=	XP_011534378.1:p.Ile201=
XM_011536077.1:c.601A=	XP_011534379.1:p.Ile201=
XR_245546.1:n.1018-5900A=
XM_005267106.5:c.664A=	XP_005267163.1:p.Ile222=
XM_011536075.2:c.601A=	XP_011534377.1:p.Ile201=
XM_011536076.3:c.601A=	XP_011534378.1:p.Ile201=
XM_017011203.2:c.601A=	XP_016866692.1:p.Ile201=
XR_001743588.1:n.1018-136A=
XR_001743589.1:n.1018-5900A=
NM_021977.4:c.1057A= MANE Select	NP_068812.1:p.Ile353=