Canonical Allele Identifier: CA1677059412

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1788382391

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437365del , CM000668.2:g.160437365del	GRCh38
NC_000006.11:g.160858397del , CM000668.1:g.160858397del	GRCh37
NC_000006.10:g.160778387del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1288+154del MANE Select	ENSP00000275300.2:n.1288+154del
ENST00000275300.2:c.1288+154del	ENSP00000275300.2:n.1288+154del
NM_021977.3:c.1288+154del	NP_068812.1:n.1288+154del
XM_005267106.3:c.895+154del	XP_005267163.1:n.895+154del
XM_011536075.1:c.832+154del	XP_011534377.1:n.832+154del
XM_011536076.1:c.832+154del	XP_011534378.1:n.832+154del
XM_011536077.1:c.832+154del	XP_011534379.1:n.832+154del
XR_245546.1:n.1018-5396del
XM_005267106.5:c.895+154del	XP_005267163.1:n.895+154del
XM_011536075.2:c.832+154del	XP_011534377.1:n.832+154del
XM_011536076.3:c.832+154del	XP_011534378.1:n.832+154del
XM_017011203.2:c.832+154del	XP_016866692.1:n.832+154del
XR_001743588.1:n.1232+154del
XR_001743589.1:n.1018-5396del
NM_021977.4:c.1288+154del MANE Select	NP_068812.1:n.1288+154del