Canonical Allele Identifier: CA2681074641

Gene: SLC22A3

Linked Data

• gnomAD v4: 6-160437350-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437350T>A , CM000668.2:g.160437350T>A	GRCh38
NC_000006.11:g.160858382T>A , CM000668.1:g.160858382T>A	GRCh37
NC_000006.10:g.160778372T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1288+139T>A MANE Select	ENSP00000275300.2:n.1288+139T>A
ENST00000275300.2:c.1288+139T>A	ENSP00000275300.2:n.1288+139T>A
NM_021977.3:c.1288+139T>A	NP_068812.1:n.1288+139T>A
XM_005267106.3:c.895+139T>A	XP_005267163.1:n.895+139T>A
XM_011536075.1:c.832+139T>A	XP_011534377.1:n.832+139T>A
XM_011536076.1:c.832+139T>A	XP_011534378.1:n.832+139T>A
XM_011536077.1:c.832+139T>A	XP_011534379.1:n.832+139T>A
XR_245546.1:n.1018-5411T>A
XM_005267106.5:c.895+139T>A	XP_005267163.1:n.895+139T>A
XM_011536075.2:c.832+139T>A	XP_011534377.1:n.832+139T>A
XM_011536076.3:c.832+139T>A	XP_011534378.1:n.832+139T>A
XM_017011203.2:c.832+139T>A	XP_016866692.1:n.832+139T>A
XR_001743588.1:n.1232+139T>A
XR_001743589.1:n.1018-5411T>A
NM_021977.4:c.1288+139T>A MANE Select	NP_068812.1:n.1288+139T>A