Canonical Allele Identifier: CA366345773
Gene: SLC22A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160437002C>A , CM000668.2:g.160437002C>A GRCh38
NC_000006.11:g.160858034C>A , CM000668.1:g.160858034C>A GRCh37
NC_000006.10:g.160778024C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000275300.3:c.1079C>A MANE Select ENSP00000275300.2:p.Thr360Lys
ENST00000275300.2:c.1079C>A ENSP00000275300.2:p.Thr360Lys
NM_021977.3:c.1079C>A NP_068812.1:p.Thr360Lys
XM_005267106.3:c.686C>A XP_005267163.1:p.Thr229Lys
XM_011536075.1:c.623C>A XP_011534377.1:p.Thr208Lys
XM_011536076.1:c.623C>A XP_011534378.1:p.Thr208Lys
XM_011536077.1:c.623C>A XP_011534379.1:p.Thr208Lys
XR_245546.1:n.1018-5759C>A
XM_005267106.5:c.686C>A XP_005267163.1:p.Thr229Lys
XM_011536075.2:c.623C>A XP_011534377.1:p.Thr208Lys
XM_011536076.3:c.623C>A XP_011534378.1:p.Thr208Lys
XM_017011203.2:c.623C>A XP_016866692.1:p.Thr208Lys
XR_001743588.1:n.1023C>A
XR_001743589.1:n.1018-5759C>A
NM_021977.4:c.1079C>A MANE Select NP_068812.1:p.Thr360Lys