Canonical Allele Identifier: CA2580575202

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160442500T>A , CM000668.2:g.160442500T>A	GRCh38
NC_000006.11:g.160863532T>A , CM000668.1:g.160863532T>A	GRCh37
NC_000006.10:g.160783522T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275300.3:c.1289-261T>A MANE Select	ENSP00000275300.2:n.1289-261T>A
ENST00000275300.2:c.1289-261T>A	ENSP00000275300.2:n.1289-261T>A
NM_021977.3:c.1289-261T>A	NP_068812.1:n.1289-261T>A
XM_005267106.3:c.896-261T>A	XP_005267163.1:n.896-261T>A
XM_011536075.1:c.833-261T>A	XP_011534377.1:n.833-261T>A
XM_011536076.1:c.833-261T>A	XP_011534378.1:n.833-261T>A
XM_011536077.1:c.833-261T>A	XP_011534379.1:n.833-261T>A
XR_245546.1:n.1018-261T>A
XM_005267106.5:c.896-261T>A	XP_005267163.1:n.896-261T>A
XM_011536075.2:c.833-261T>A	XP_011534377.1:n.833-261T>A
XM_011536076.3:c.833-261T>A	XP_011534378.1:n.833-261T>A
XM_017011203.2:c.833-261T>A	XP_016866692.1:n.833-261T>A
XR_001743588.1:n.1233-261T>A
XR_001743589.1:n.1018-261T>A
NM_021977.4:c.1289-261T>A MANE Select	NP_068812.1:n.1289-261T>A