Canonical Allele Identifier: CA2581615359

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160387116C>G , CM000668.2:g.160387116C>G	GRCh38
NC_000006.11:g.160808148C>G , CM000668.1:g.160808148C>G	GRCh37
NC_000006.10:g.160728138C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275300.3:c.430-10863C>G MANE Select	ENSP00000275300.2:n.430-10863C>G
ENST00000275300.2:c.430-10863C>G	ENSP00000275300.2:n.430-10863C>G
NM_021977.3:c.430-10863C>G	NP_068812.1:n.430-10863C>G
XM_005267106.3:c.37-10863C>G	XP_005267163.1:n.37-10863C>G
XM_005267107.2:c.430-10863C>G	XP_005267164.1:n.430-10863C>G
XM_011536076.1:c.-27-10863C>G	XP_011534378.1:n.-27-10863C>G
XM_011536077.1:c.-27-10863C>G	XP_011534379.1:n.-27-10863C>G
XM_011536078.1:c.430-10863C>G	XP_011534380.1:n.430-10863C>G
XR_245546.1:n.472-10863C>G
XR_943187.1:n.4881G>C
XM_005267106.5:c.37-10863C>G	XP_005267163.1:n.37-10863C>G
XM_005267107.3:c.430-10863C>G	XP_005267164.1:n.430-10863C>G
XM_011536075.2:c.-5407C>G	XP_011534377.1:n.-5407C>G
XM_011536076.3:c.-27-10863C>G	XP_011534378.1:n.-27-10863C>G
XM_017011203.2:c.-27-10863C>G	XP_016866692.1:n.-27-10863C>G
XR_001743588.1:n.472-10863C>G
XR_001743589.1:n.472-10863C>G
NM_021977.4:c.430-10863C>G MANE Select	NP_068812.1:n.430-10863C>G