Canonical Allele Identifier: CA2681074598

Gene: SLC22A3

Linked Data

• gnomAD v4: 6-160437285-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437285C>A , CM000668.2:g.160437285C>A	GRCh38
NC_000006.11:g.160858317C>A , CM000668.1:g.160858317C>A	GRCh37
NC_000006.10:g.160778307C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1288+74C>A MANE Select	ENSP00000275300.2:n.1288+74C>A
ENST00000275300.2:c.1288+74C>A	ENSP00000275300.2:n.1288+74C>A
NM_021977.3:c.1288+74C>A	NP_068812.1:n.1288+74C>A
XM_005267106.3:c.895+74C>A	XP_005267163.1:n.895+74C>A
XM_011536075.1:c.832+74C>A	XP_011534377.1:n.832+74C>A
XM_011536076.1:c.832+74C>A	XP_011534378.1:n.832+74C>A
XM_011536077.1:c.832+74C>A	XP_011534379.1:n.832+74C>A
XR_245546.1:n.1018-5476C>A
XM_005267106.5:c.895+74C>A	XP_005267163.1:n.895+74C>A
XM_011536075.2:c.832+74C>A	XP_011534377.1:n.832+74C>A
XM_011536076.3:c.832+74C>A	XP_011534378.1:n.832+74C>A
XM_017011203.2:c.832+74C>A	XP_016866692.1:n.832+74C>A
XR_001743588.1:n.1232+74C>A
XR_001743589.1:n.1018-5476C>A
NM_021977.4:c.1288+74C>A MANE Select	NP_068812.1:n.1288+74C>A