Canonical Allele Identifier: CA1096541992
Gene: SLC22A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160387117_160387119del , CM000668.2:g.160387117_160387119del GRCh38
NC_000006.11:g.160808149_160808151del , CM000668.1:g.160808149_160808151del GRCh37
NC_000006.10:g.160728139_160728141del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000275300.3:c.430-10862_430-10860del MANE Select ENSP00000275300.2:n.430-10862_430-10860de...
ENST00000275300.2:c.430-10862_430-10860del ENSP00000275300.2:n.430-10862_430-10860de...
NM_021977.3:c.430-10862_430-10860del NP_068812.1:n.430-10862_430-10860del
XM_005267106.3:c.37-10862_37-10860del XP_005267163.1:n.37-10862_37-10860del
XM_005267107.2:c.430-10862_430-10860del XP_005267164.1:n.430-10862_430-10860del
XM_011536076.1:c.-27-10862_-27-10860del XP_011534378.1:n.-27-10862_-27-10860del
XM_011536077.1:c.-27-10862_-27-10860del XP_011534379.1:n.-27-10862_-27-10860del
XM_011536078.1:c.430-10862_430-10860del XP_011534380.1:n.430-10862_430-10860del
XR_245546.1:n.472-10862_472-10860del
XR_943187.1:n.4878_4880del
XM_005267106.5:c.37-10862_37-10860del XP_005267163.1:n.37-10862_37-10860del
XM_005267107.3:c.430-10862_430-10860del XP_005267164.1:n.430-10862_430-10860del
XM_011536075.2:c.-5406_-5404del XP_011534377.1:n.-5406_-5404del
XM_011536076.3:c.-27-10862_-27-10860del XP_011534378.1:n.-27-10862_-27-10860del
XM_017011203.2:c.-27-10862_-27-10860del XP_016866692.1:n.-27-10862_-27-10860del
XR_001743588.1:n.472-10862_472-10860del
XR_001743589.1:n.472-10862_472-10860del
NM_021977.4:c.430-10862_430-10860del MANE Select NP_068812.1:n.430-10862_430-10860del