Canonical Allele Identifier: CA2681074530
Gene: SLC22A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160436863_160436868del , CM000668.2:g.160436863_160436868del GRCh38
NC_000006.11:g.160857895_160857900del , CM000668.1:g.160857895_160857900del GRCh37
NC_000006.10:g.160777885_160777890del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000275300.3:c.1059_1064del MANE Select ENSP00000275300.2:p.Ile353_Leu354del
ENST00000275300.2:c.1059_1064del ENSP00000275300.2:p.Ile353_Leu354del
NM_021977.3:c.1059_1064del NP_068812.1:p.Ile353_Leu354del
XM_005267106.3:c.666_671del XP_005267163.1:p.Ile222_Leu223del
XM_011536075.1:c.603_608del XP_011534377.1:p.Ile201_Leu202del
XM_011536076.1:c.603_608del XP_011534378.1:p.Ile201_Leu202del
XM_011536077.1:c.603_608del XP_011534379.1:p.Ile201_Leu202del
XR_245546.1:n.1018-5898_1018-5893del
XM_005267106.5:c.666_671del XP_005267163.1:p.Ile222_Leu223del
XM_011536075.2:c.603_608del XP_011534377.1:p.Ile201_Leu202del
XM_011536076.3:c.603_608del XP_011534378.1:p.Ile201_Leu202del
XM_017011203.2:c.603_608del XP_016866692.1:p.Ile201_Leu202del
XR_001743588.1:n.1018-134_1018-129del
XR_001743589.1:n.1018-5898_1018-5893del
NM_021977.4:c.1059_1064del MANE Select NP_068812.1:p.Ile353_Leu354del