Canonical Allele Identifier: CA1677027739
Gene: SLC22A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160419161_160419164delinsTTAC , CM000668.2:g.160419161_160419164delinsTTAC GRCh38
NC_000006.11:g.160840193_160840196delinsTTAC , CM000668.1:g.160840193_160840196delinsTTAC GRCh37
NC_000006.10:g.160760183_160760186delinsTTAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000275300.3:c.975+8315_975+8318delinsTTAC MANE Select ENSP00000275300.2:n.975+8315_975+8318delinsTTAC
ENST00000275300.2:c.975+8315_975+8318delinsTTAC ENSP00000275300.2:n.975+8315_975+8318delinsTTAC
NM_021977.3:c.975+8315_975+8318delinsTTAC NP_068812.1:n.975+8315_975+8318delinsTTAC
XM_005267106.3:c.582+8315_582+8318delinsTTAC XP_005267163.1:n.582+8315_582+8318delinsTTAC
XM_005267107.2:c.976-6690_976-6687delinsTTAC XP_005267164.1:n.976-6690_976-6687delinsTTAC
XM_011536075.1:c.519+8315_519+8318delinsTTAC XP_011534377.1:n.519+8315_519+8318delinsTTAC
XM_011536076.1:c.519+8315_519+8318delinsTTAC XP_011534378.1:n.519+8315_519+8318delinsTTAC
XM_011536077.1:c.519+8315_519+8318delinsTTAC XP_011534379.1:n.519+8315_519+8318delinsTTAC
XM_011536078.1:c.975+8315_975+8318delinsTTAC XP_011534380.1:n.975+8315_975+8318delinsTTAC
XR_245546.1:n.1017+8315_1017+8318delinsTTAC
XM_005267106.5:c.582+8315_582+8318delinsTTAC XP_005267163.1:n.582+8315_582+8318delinsTTAC
XM_005267107.3:c.976-6690_976-6687delinsTTAC XP_005267164.1:n.976-6690_976-6687delinsTTAC
XM_011536075.2:c.519+8315_519+8318delinsTTAC XP_011534377.1:n.519+8315_519+8318delinsTTAC
XM_011536076.3:c.519+8315_519+8318delinsTTAC XP_011534378.1:n.519+8315_519+8318delinsTTAC
XM_017011203.2:c.519+8315_519+8318delinsTTAC XP_016866692.1:n.519+8315_519+8318delinsTTAC
XR_001743588.1:n.1017+8315_1017+8318delinsTTAC
XR_001743589.1:n.1017+8315_1017+8318delinsTTAC
NM_021977.4:c.975+8315_975+8318delinsTTAC MANE Select NP_068812.1:n.975+8315_975+8318delinsTTAC