Canonical Allele Identifier: CA1677027769
Gene: SLC22A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160419200_160419201delinsTC , CM000668.2:g.160419200_160419201delinsTC GRCh38
NC_000006.11:g.160840232_160840233delinsTC , CM000668.1:g.160840232_160840233delinsTC GRCh37
NC_000006.10:g.160760222_160760223delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000275300.3:c.975+8354_975+8355delinsTC MANE Select ENSP00000275300.2:n.975+8354_975+8355delinsTC
ENST00000275300.2:c.975+8354_975+8355delinsTC ENSP00000275300.2:n.975+8354_975+8355delinsTC
NM_021977.3:c.975+8354_975+8355delinsTC NP_068812.1:n.975+8354_975+8355delinsTC
XM_005267106.3:c.582+8354_582+8355delinsTC XP_005267163.1:n.582+8354_582+8355delinsTC
XM_005267107.2:c.976-6651_976-6650delinsTC XP_005267164.1:n.976-6651_976-6650delinsTC
XM_011536075.1:c.519+8354_519+8355delinsTC XP_011534377.1:n.519+8354_519+8355delinsTC
XM_011536076.1:c.519+8354_519+8355delinsTC XP_011534378.1:n.519+8354_519+8355delinsTC
XM_011536077.1:c.519+8354_519+8355delinsTC XP_011534379.1:n.519+8354_519+8355delinsTC
XM_011536078.1:c.975+8354_975+8355delinsTC XP_011534380.1:n.975+8354_975+8355delinsTC
XR_245546.1:n.1017+8354_1017+8355delinsTC
XM_005267106.5:c.582+8354_582+8355delinsTC XP_005267163.1:n.582+8354_582+8355delinsTC
XM_005267107.3:c.976-6651_976-6650delinsTC XP_005267164.1:n.976-6651_976-6650delinsTC
XM_011536075.2:c.519+8354_519+8355delinsTC XP_011534377.1:n.519+8354_519+8355delinsTC
XM_011536076.3:c.519+8354_519+8355delinsTC XP_011534378.1:n.519+8354_519+8355delinsTC
XM_017011203.2:c.519+8354_519+8355delinsTC XP_016866692.1:n.519+8354_519+8355delinsTC
XR_001743588.1:n.1017+8354_1017+8355delinsTC
XR_001743589.1:n.1017+8354_1017+8355delinsTC
NM_021977.4:c.975+8354_975+8355delinsTC MANE Select NP_068812.1:n.975+8354_975+8355delinsTC