Canonical Allele Identifier: CA1677059375

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1788379348
• gnomAD v4: 6-160437275-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437278_160437279dup , CM000668.2:g.160437278_160437279dup	GRCh38
NC_000006.11:g.160858310_160858311dup , CM000668.1:g.160858310_160858311dup	GRCh37
NC_000006.10:g.160778300_160778301dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1288+67_1288+68dup MANE Select	ENSP00000275300.2:n.1288+67_1288+68dup
ENST00000275300.2:c.1288+67_1288+68dup	ENSP00000275300.2:n.1288+67_1288+68dup
NM_021977.3:c.1288+67_1288+68dup	NP_068812.1:n.1288+67_1288+68dup
XM_005267106.3:c.895+67_895+68dup	XP_005267163.1:n.895+67_895+68dup
XM_011536075.1:c.832+67_832+68dup	XP_011534377.1:n.832+67_832+68dup
XM_011536076.1:c.832+67_832+68dup	XP_011534378.1:n.832+67_832+68dup
XM_011536077.1:c.832+67_832+68dup	XP_011534379.1:n.832+67_832+68dup
XR_245546.1:n.1018-5483_1018-5482dup
XM_005267106.5:c.895+67_895+68dup	XP_005267163.1:n.895+67_895+68dup
XM_011536075.2:c.832+67_832+68dup	XP_011534377.1:n.832+67_832+68dup
XM_011536076.3:c.832+67_832+68dup	XP_011534378.1:n.832+67_832+68dup
XM_017011203.2:c.832+67_832+68dup	XP_016866692.1:n.832+67_832+68dup
XR_001743588.1:n.1232+67_1232+68dup
XR_001743589.1:n.1018-5483_1018-5482dup
NM_021977.4:c.1288+67_1288+68dup MANE Select	NP_068812.1:n.1288+67_1288+68dup