Canonical Allele Identifier: CA1677032832

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160368264A= , CM000668.2:g.160368264A=	GRCh38
NC_000006.11:g.160789296A= , CM000668.1:g.160789296A=	GRCh37
NC_000006.10:g.160709286A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.429+19416A= MANE Select	ENSP00000275300.2:n.429+19416A=
ENST00000275300.2:c.429+19416A=	ENSP00000275300.2:n.429+19416A=
NM_021977.3:c.429+19416A=	NP_068812.1:n.429+19416A=
XM_005267106.3:c.36+19206A=	XP_005267163.1:n.36+19206A=
XM_005267107.2:c.429+19416A=	XP_005267164.1:n.429+19416A=
XM_011536076.1:c.-28+19079A=	XP_011534378.1:n.-28+19079A=
XM_011536077.1:c.-28+17594A=	XP_011534379.1:n.-28+17594A=
XM_011536078.1:c.429+19416A=	XP_011534380.1:n.429+19416A=
XR_245546.1:n.471+19416A=
XM_005267106.5:c.36+19206A=	XP_005267163.1:n.36+19206A=
XM_005267107.3:c.429+19416A=	XP_005267164.1:n.429+19416A=
XM_011536076.3:c.-28+19079A=	XP_011534378.1:n.-28+19079A=
XM_017011203.2:c.-28+17594A=	XP_016866692.1:n.-28+17594A=
XR_001743588.1:n.471+19416A=
XR_001743589.1:n.471+19416A=
NM_021977.4:c.429+19416A= MANE Select	NP_068812.1:n.429+19416A=