Canonical Allele Identifier: CA2681074593

Gene: SLC22A3

Linked Data

• gnomAD v4: 6-160437279-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437282del , CM000668.2:g.160437282del	GRCh38
NC_000006.11:g.160858314del , CM000668.1:g.160858314del	GRCh37
NC_000006.10:g.160778304del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1288+71del MANE Select	ENSP00000275300.2:n.1288+71del
ENST00000275300.2:c.1288+71del	ENSP00000275300.2:n.1288+71del
NM_021977.3:c.1288+71del	NP_068812.1:n.1288+71del
XM_005267106.3:c.895+71del	XP_005267163.1:n.895+71del
XM_011536075.1:c.832+71del	XP_011534377.1:n.832+71del
XM_011536076.1:c.832+71del	XP_011534378.1:n.832+71del
XM_011536077.1:c.832+71del	XP_011534379.1:n.832+71del
XR_245546.1:n.1018-5479del
XM_005267106.5:c.895+71del	XP_005267163.1:n.895+71del
XM_011536075.2:c.832+71del	XP_011534377.1:n.832+71del
XM_011536076.3:c.832+71del	XP_011534378.1:n.832+71del
XM_017011203.2:c.832+71del	XP_016866692.1:n.832+71del
XR_001743588.1:n.1232+71del
XR_001743589.1:n.1018-5479del
NM_021977.4:c.1288+71del MANE Select	NP_068812.1:n.1288+71del