Canonical Allele Identifier: CA2575234502
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097639_119097640del , CM000673.2:g.119097639_119097640del GRCh38
NC_000011.9:g.118968349_118968350del , CM000673.1:g.118968349_118968350del GRCh37
NC_000011.8:g.118473559_118473560del NCBI36
NG_008918.1:g.9436_9437del

Transcript Alleles

HGVS Amino-acid Change
ENST00000445653.6:n.976-89_976-88del
ENST00000524658.2:n.957-89_957-88del
ENST00000530052.2:n.1874_1875del
ENST00000682191.1:n.1334_1335del
ENST00000682192.1:n.1120-89_1120-88del
ENST00000682232.1:c.*622+215_*622+216del ENSP00000507302.1:n.*622+215_*622+216del
ENST00000682326.1:c.917+215_917+216del ENSP00000508129.1:n.917+215_917+216del
ENST00000682404.1:n.2019-89_2019-88del
ENST00000682517.1:n.2233_2234del
ENST00000682652.1:n.2103_2104del
ENST00000682665.1:n.1529_1530del
ENST00000682691.1:n.1529_1530del
ENST00000682791.1:c.831-89_831-88del ENSP00000507312.1:n.831-89_831-88del
ENST00000682811.1:c.800-89_800-88del ENSP00000508196.1:n.800-89_800-88del
ENST00000682883.1:n.1032-343_1032-342del
ENST00000682946.1:c.729-89_729-88del ENSP00000506856.1:n.729-89_729-88del
ENST00000683143.1:c.*623-89_*623-88del ENSP00000507168.1:n.*623-89_*623-88del
ENST00000683373.1:n.1334_1335del
ENST00000683558.1:n.1334_1335del
ENST00000683567.1:n.1027-89_1027-88del
ENST00000683955.1:n.1674-89_1674-88del
ENST00000684142.1:c.*593-89_*593-88del ENSP00000508008.1:n.*593-89_*593-88del
ENST00000684252.1:n.1315-89_1315-88del
ENST00000684255.1:c.*623-89_*623-88del ENSP00000507398.1:n.*623-89_*623-88del
ENST00000684315.1:n.1651-89_1651-88del
ENST00000684345.1:c.*807_*808del ENSP00000507163.1:n.*807_*808del
ENST00000684499.1:c.*1023-89_*1023-88del ENSP00000506800.1:n.*1023-89_*1023-88del
ENST00000684682.1:c.*560_*561del ENSP00000507326.1:n.*560_*561del
ENST00000354202.9:c.918-89_918-88del MANE Select ENSP00000346142.4:n.918-89_918-88del
ENST00000636404.1:c.233-577_233-576del
ENST00000638850.1:c.422-89_422-88del
ENST00000639704.1:c.825-89_825-88del ENSP00000491336.1:n.825-89_825-88del
ENST00000640102.1:c.*571-89_*571-88del ENSP00000492027.1:n.*571-89_*571-88del
ENST00000640747.1:c.*593-89_*593-88del ENSP00000492730.1:n.*593-89_*593-88del
ENST00000354202.8:c.918-89_918-88del ENSP00000346142.4:n.918-89_918-88del
ENST00000392834.7:c.*623-89_*623-88del ENSP00000376579.3:n.*623-89_*623-88del
ENST00000409993.6:c.918-89_918-88del ENSP00000386597.2:n.918-89_918-88del
ENST00000414373.5:c.*475-343_*475-342del ENSP00000402019.1:n.*475-343_*475-342del
ENST00000442480.1:c.650-89_650-88del ENSP00000406591.1:n.650-89_650-88del
ENST00000461999.1:n.996_997del
ENST00000481084.5:n.1547-89_1547-88del
ENST00000524658.1:n.223-89_223-88del
ENST00000525456.5:n.732-89_732-88del
NM_001382.3:c.918-89_918-88del NP_001373.2:n.918-89_918-88del
XM_005271422.2:c.918-89_918-88del XP_005271479.1:n.918-89_918-88del
XM_011542648.1:c.597-89_597-88del XP_011540950.1:n.597-89_597-88del
XR_947801.1:n.1165-343_1165-342del
XM_005271422.3:c.918-89_918-88del XP_005271479.1:n.918-89_918-88del
XM_011542648.2:c.597-89_597-88del XP_011540950.1:n.597-89_597-88del
XM_017017293.2:c.597-89_597-88del XP_016872782.1:n.597-89_597-88del
XM_017017294.2:c.729-89_729-88del XP_016872783.1:n.729-89_729-88del
XM_017017295.1:c.402-89_402-88del XP_016872784.1:n.402-89_402-88del
XR_001747785.2:n.952-89_952-88del
XR_947801.2:n.952-343_952-342del
NM_001382.4:c.918-89_918-88del MANE Select NP_001373.2:n.918-89_918-88del