Canonical Allele Identifier: CA2575234492
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097595del , CM000673.2:g.119097595del GRCh38
NC_000011.9:g.118968305del , CM000673.1:g.118968305del GRCh37
NC_000011.8:g.118473515del NCBI36
NG_008918.1:g.9482del

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.976-43del
ENST00000524658.2:n.957-43del
ENST00000530052.2:n.1920del
ENST00000682191.1:n.1380del
ENST00000682192.1:n.1120-43del
ENST00000682232.1:c.*622+261del ENSP00000507302.1:n.*622+261del
ENST00000682326.1:c.917+261del ENSP00000508129.1:n.917+261del
ENST00000682404.1:n.2019-43del
ENST00000682517.1:n.2279del
ENST00000682652.1:n.2149del
ENST00000682665.1:n.1575del
ENST00000682691.1:n.1575del
ENST00000682791.1:c.831-43del ENSP00000507312.1:n.831-43del
ENST00000682811.1:c.800-43del ENSP00000508196.1:n.800-43del
ENST00000682883.1:n.1032-297del
ENST00000682946.1:c.729-43del ENSP00000506856.1:n.729-43del
ENST00000683143.1:c.*623-43del ENSP00000507168.1:n.*623-43del
ENST00000683373.1:n.1380del
ENST00000683558.1:n.1380del
ENST00000683567.1:n.1027-43del
ENST00000683955.1:n.1674-43del
ENST00000684142.1:c.*593-43del ENSP00000508008.1:n.*593-43del
ENST00000684252.1:n.1315-43del
ENST00000684255.1:c.*623-43del ENSP00000507398.1:n.*623-43del
ENST00000684315.1:n.1651-43del
ENST00000684345.1:c.*853del ENSP00000507163.1:n.*853del
ENST00000684499.1:c.*1023-43del ENSP00000506800.1:n.*1023-43del
ENST00000684682.1:c.*606del ENSP00000507326.1:n.*606del
ENST00000354202.9:c.918-43del MANE Select ENSP00000346142.4:n.918-43del
ENST00000636404.1:c.233-531del
ENST00000638850.1:c.422-43del
ENST00000639704.1:c.825-43del ENSP00000491336.1:n.825-43del
ENST00000640102.1:c.*571-43del ENSP00000492027.1:n.*571-43del
ENST00000640747.1:c.*593-43del ENSP00000492730.1:n.*593-43del
ENST00000354202.8:c.918-43del ENSP00000346142.4:n.918-43del
ENST00000392834.7:c.*623-43del ENSP00000376579.3:n.*623-43del
ENST00000409993.6:c.918-43del ENSP00000386597.2:n.918-43del
ENST00000414373.5:c.*475-297del ENSP00000402019.1:n.*475-297del
ENST00000442480.1:c.650-43del ENSP00000406591.1:n.650-43del
ENST00000461999.1:n.1042del
ENST00000481084.5:n.1547-43del
ENST00000524658.1:n.223-43del
ENST00000525456.5:n.732-43del
NM_001382.3:c.918-43del NP_001373.2:n.918-43del
XM_005271422.2:c.918-43del XP_005271479.1:n.918-43del
XM_011542648.1:c.597-43del XP_011540950.1:n.597-43del
XR_947801.1:n.1165-297del
XM_005271422.3:c.918-43del XP_005271479.1:n.918-43del
XM_011542648.2:c.597-43del XP_011540950.1:n.597-43del
XM_017017293.2:c.597-43del XP_016872782.1:n.597-43del
XM_017017294.2:c.729-43del XP_016872783.1:n.729-43del
XM_017017295.1:c.402-43del XP_016872784.1:n.402-43del
XR_001747785.2:n.952-43del
XR_947801.2:n.952-297del
NM_001382.4:c.918-43del MANE Select NP_001373.2:n.918-43del