Canonical Allele Identifier: CA1096534753
Gene: SLC22A3 HGNC NCBI

Linked Data

dbSNP Id: rs1787627029

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160419163_160419165del , CM000668.2:g.160419163_160419165del GRCh38
NC_000006.11:g.160840195_160840197del , CM000668.1:g.160840195_160840197del GRCh37
NC_000006.10:g.160760185_160760187del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000275300.3:c.975+8317_975+8319del MANE Select ENSP00000275300.2:n.975+8317_975+8319del
ENST00000275300.2:c.975+8317_975+8319del ENSP00000275300.2:n.975+8317_975+8319del
NM_021977.3:c.975+8317_975+8319del NP_068812.1:n.975+8317_975+8319del
XM_005267106.3:c.582+8317_582+8319del XP_005267163.1:n.582+8317_582+8319del
XM_005267107.2:c.976-6688_976-6686del XP_005267164.1:n.976-6688_976-6686del
XM_011536075.1:c.519+8317_519+8319del XP_011534377.1:n.519+8317_519+8319del
XM_011536076.1:c.519+8317_519+8319del XP_011534378.1:n.519+8317_519+8319del
XM_011536077.1:c.519+8317_519+8319del XP_011534379.1:n.519+8317_519+8319del
XM_011536078.1:c.975+8317_975+8319del XP_011534380.1:n.975+8317_975+8319del
XR_245546.1:n.1017+8317_1017+8319del
XM_005267106.5:c.582+8317_582+8319del XP_005267163.1:n.582+8317_582+8319del
XM_005267107.3:c.976-6688_976-6686del XP_005267164.1:n.976-6688_976-6686del
XM_011536075.2:c.519+8317_519+8319del XP_011534377.1:n.519+8317_519+8319del
XM_011536076.3:c.519+8317_519+8319del XP_011534378.1:n.519+8317_519+8319del
XM_017011203.2:c.519+8317_519+8319del XP_016866692.1:n.519+8317_519+8319del
XR_001743588.1:n.1017+8317_1017+8319del
XR_001743589.1:n.1017+8317_1017+8319del
NM_021977.4:c.975+8317_975+8319del MANE Select NP_068812.1:n.975+8317_975+8319del