Canonical Allele Identifier: CA1677048127

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160387213C= , CM000668.2:g.160387213C=	GRCh38
NC_000006.11:g.160808245C= , CM000668.1:g.160808245C=	GRCh37
NC_000006.10:g.160728235C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.430-10766C= MANE Select	ENSP00000275300.2:n.430-10766C=
ENST00000275300.2:c.430-10766C=	ENSP00000275300.2:n.430-10766C=
NM_021977.3:c.430-10766C=	NP_068812.1:n.430-10766C=
XM_005267106.3:c.37-10766C=	XP_005267163.1:n.37-10766C=
XM_005267107.2:c.430-10766C=	XP_005267164.1:n.430-10766C=
XM_011536076.1:c.-27-10766C=	XP_011534378.1:n.-27-10766C=
XM_011536077.1:c.-27-10766C=	XP_011534379.1:n.-27-10766C=
XM_011536078.1:c.430-10766C=	XP_011534380.1:n.430-10766C=
XR_245546.1:n.472-10766C=
XR_943187.1:n.4784G=
XM_005267106.5:c.37-10766C=	XP_005267163.1:n.37-10766C=
XM_005267107.3:c.430-10766C=	XP_005267164.1:n.430-10766C=
XM_011536075.2:c.-5310C=	XP_011534377.1:n.-5310C=
XM_011536076.3:c.-27-10766C=	XP_011534378.1:n.-27-10766C=
XM_017011203.2:c.-27-10766C=	XP_016866692.1:n.-27-10766C=
XR_001743588.1:n.472-10766C=
XR_001743589.1:n.472-10766C=
NM_021977.4:c.430-10766C= MANE Select	NP_068812.1:n.430-10766C=