Canonical Allele Identifier: CA1677047966
Gene: SLC22A3 HGNC NCBI

Linked Data

dbSNP Id: rs1786048297
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160387032_160387035del , CM000668.2:g.160387032_160387035del GRCh38
NC_000006.11:g.160808064_160808067del , CM000668.1:g.160808064_160808067del GRCh37
NC_000006.10:g.160728054_160728057del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000275300.3:c.430-10947_430-10944del MANE Select ENSP00000275300.2:n.430-10947_430-10944de...
ENST00000275300.2:c.430-10947_430-10944del ENSP00000275300.2:n.430-10947_430-10944de...
NM_021977.3:c.430-10947_430-10944del NP_068812.1:n.430-10947_430-10944del
XM_005267106.3:c.37-10947_37-10944del XP_005267163.1:n.37-10947_37-10944del
XM_005267107.2:c.430-10947_430-10944del XP_005267164.1:n.430-10947_430-10944del
XM_011536076.1:c.-27-10947_-27-10944del XP_011534378.1:n.-27-10947_-27-10944del
XM_011536077.1:c.-27-10947_-27-10944del XP_011534379.1:n.-27-10947_-27-10944del
XM_011536078.1:c.430-10947_430-10944del XP_011534380.1:n.430-10947_430-10944del
XR_245546.1:n.472-10947_472-10944del
XR_943187.1:n.4963_4966del
XM_005267106.5:c.37-10947_37-10944del XP_005267163.1:n.37-10947_37-10944del
XM_005267107.3:c.430-10947_430-10944del XP_005267164.1:n.430-10947_430-10944del
XM_011536075.2:c.-5491_-5488del XP_011534377.1:n.-5491_-5488del
XM_011536076.3:c.-27-10947_-27-10944del XP_011534378.1:n.-27-10947_-27-10944del
XM_017011203.2:c.-27-10947_-27-10944del XP_016866692.1:n.-27-10947_-27-10944del
XR_001743588.1:n.472-10947_472-10944del
XR_001743589.1:n.472-10947_472-10944del
NM_021977.4:c.430-10947_430-10944del MANE Select NP_068812.1:n.430-10947_430-10944del
Search 100 bp 5'
Search 100 bp 3'