Canonical Allele Identifier: CA1677048067
Gene: SLC22A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160387129C= , CM000668.2:g.160387129C= GRCh38
NC_000006.11:g.160808161C= , CM000668.1:g.160808161C= GRCh37
NC_000006.10:g.160728151C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000275300.3:c.430-10850C= MANE Select ENSP00000275300.2:n.430-10850C=
ENST00000275300.2:c.430-10850C= ENSP00000275300.2:n.430-10850C=
NM_021977.3:c.430-10850C= NP_068812.1:n.430-10850C=
XM_005267106.3:c.37-10850C= XP_005267163.1:n.37-10850C=
XM_005267107.2:c.430-10850C= XP_005267164.1:n.430-10850C=
XM_011536076.1:c.-27-10850C= XP_011534378.1:n.-27-10850C=
XM_011536077.1:c.-27-10850C= XP_011534379.1:n.-27-10850C=
XM_011536078.1:c.430-10850C= XP_011534380.1:n.430-10850C=
XR_245546.1:n.472-10850C=
XR_943187.1:n.4868G=
XM_005267106.5:c.37-10850C= XP_005267163.1:n.37-10850C=
XM_005267107.3:c.430-10850C= XP_005267164.1:n.430-10850C=
XM_011536075.2:c.-5394C= XP_011534377.1:n.-5394C=
XM_011536076.3:c.-27-10850C= XP_011534378.1:n.-27-10850C=
XM_017011203.2:c.-27-10850C= XP_016866692.1:n.-27-10850C=
XR_001743588.1:n.472-10850C=
XR_001743589.1:n.472-10850C=
NM_021977.4:c.430-10850C= MANE Select NP_068812.1:n.430-10850C=