Canonical Allele Identifier: CA2793833495
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097602_119097604del , CM000673.2:g.119097602_119097604del GRCh38
NC_000011.9:g.118968312_118968314del , CM000673.1:g.118968312_118968314del GRCh37
NC_000011.8:g.118473522_118473524del NCBI36
NG_008918.1:g.9477_9479del

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.976-48_976-46del
ENST00000524658.2:n.957-48_957-46del
ENST00000530052.2:n.1915_1917del
ENST00000682191.1:n.1375_1377del
ENST00000682192.1:n.1120-48_1120-46del
ENST00000682232.1:c.*622+256_*622+258del ENSP00000507302.1:n.*622+256_*622+258del
ENST00000682326.1:c.917+256_917+258del ENSP00000508129.1:n.917+256_917+258del
ENST00000682404.1:n.2019-48_2019-46del
ENST00000682517.1:n.2274_2276del
ENST00000682652.1:n.2144_2146del
ENST00000682665.1:n.1570_1572del
ENST00000682691.1:n.1570_1572del
ENST00000682791.1:c.831-48_831-46del ENSP00000507312.1:n.831-48_831-46del
ENST00000682811.1:c.800-48_800-46del ENSP00000508196.1:n.800-48_800-46del
ENST00000682883.1:n.1032-302_1032-300del
ENST00000682946.1:c.729-48_729-46del ENSP00000506856.1:n.729-48_729-46del
ENST00000683143.1:c.*623-48_*623-46del ENSP00000507168.1:n.*623-48_*623-46del
ENST00000683373.1:n.1375_1377del
ENST00000683558.1:n.1375_1377del
ENST00000683567.1:n.1027-48_1027-46del
ENST00000683955.1:n.1674-48_1674-46del
ENST00000684142.1:c.*593-48_*593-46del ENSP00000508008.1:n.*593-48_*593-46del
ENST00000684252.1:n.1315-48_1315-46del
ENST00000684255.1:c.*623-48_*623-46del ENSP00000507398.1:n.*623-48_*623-46del
ENST00000684315.1:n.1651-48_1651-46del
ENST00000684345.1:c.*848_*850del ENSP00000507163.1:n.*848_*850del
ENST00000684499.1:c.*1023-48_*1023-46del ENSP00000506800.1:n.*1023-48_*1023-46del
ENST00000684682.1:c.*601_*603del ENSP00000507326.1:n.*601_*603del
ENST00000354202.9:c.918-48_918-46del MANE Select ENSP00000346142.4:n.918-48_918-46del
ENST00000636404.1:c.233-536_233-534del
ENST00000638850.1:c.422-48_422-46del
ENST00000639704.1:c.825-48_825-46del ENSP00000491336.1:n.825-48_825-46del
ENST00000640102.1:c.*571-48_*571-46del ENSP00000492027.1:n.*571-48_*571-46del
ENST00000640747.1:c.*593-48_*593-46del ENSP00000492730.1:n.*593-48_*593-46del
ENST00000354202.8:c.918-48_918-46del ENSP00000346142.4:n.918-48_918-46del
ENST00000392834.7:c.*623-48_*623-46del ENSP00000376579.3:n.*623-48_*623-46del
ENST00000409993.6:c.918-48_918-46del ENSP00000386597.2:n.918-48_918-46del
ENST00000414373.5:c.*475-302_*475-300del ENSP00000402019.1:n.*475-302_*475-300del
ENST00000442480.1:c.650-48_650-46del ENSP00000406591.1:n.650-48_650-46del
ENST00000461999.1:n.1037_1039del
ENST00000481084.5:n.1547-48_1547-46del
ENST00000524658.1:n.223-48_223-46del
ENST00000525456.5:n.732-48_732-46del
NM_001382.3:c.918-48_918-46del NP_001373.2:n.918-48_918-46del
XM_005271422.2:c.918-48_918-46del XP_005271479.1:n.918-48_918-46del
XM_011542648.1:c.597-48_597-46del XP_011540950.1:n.597-48_597-46del
XR_947801.1:n.1165-302_1165-300del
XM_005271422.3:c.918-48_918-46del XP_005271479.1:n.918-48_918-46del
XM_011542648.2:c.597-48_597-46del XP_011540950.1:n.597-48_597-46del
XM_017017293.2:c.597-48_597-46del XP_016872782.1:n.597-48_597-46del
XM_017017294.2:c.729-48_729-46del XP_016872783.1:n.729-48_729-46del
XM_017017295.1:c.402-48_402-46del XP_016872784.1:n.402-48_402-46del
XR_001747785.2:n.952-48_952-46del
XR_947801.2:n.952-302_952-300del
NM_001382.4:c.918-48_918-46del MANE Select NP_001373.2:n.918-48_918-46del