Canonical Allele Identifier: CA1677059174

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436840C= , CM000668.2:g.160436840C=	GRCh38
NC_000006.11:g.160857872C= , CM000668.1:g.160857872C=	GRCh37
NC_000006.10:g.160777862C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1036C= MANE Select	ENSP00000275300.2:p.Gln346=
ENST00000275300.2:c.1036C=	ENSP00000275300.2:p.Gln346=
NM_021977.3:c.1036C=	NP_068812.1:p.Gln346=
XM_005267106.3:c.643C=	XP_005267163.1:p.Gln215=
XM_011536075.1:c.580C=	XP_011534377.1:p.Gln194=
XM_011536076.1:c.580C=	XP_011534378.1:p.Gln194=
XM_011536077.1:c.580C=	XP_011534379.1:p.Gln194=
XR_245546.1:n.1018-5921C=
XM_005267106.5:c.643C=	XP_005267163.1:p.Gln215=
XM_011536075.2:c.580C=	XP_011534377.1:p.Gln194=
XM_011536076.3:c.580C=	XP_011534378.1:p.Gln194=
XM_017011203.2:c.580C=	XP_016866692.1:p.Gln194=
XR_001743588.1:n.1018-157C=
XR_001743589.1:n.1018-5921C=
NM_021977.4:c.1036C= MANE Select	NP_068812.1:p.Gln346=