Canonical Allele Identifier: CA2003808873

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097595_119097596delinsAC , CM000673.2:g.119097595_119097596delinsAC	GRCh38
NC_000011.9:g.118968305_118968306delinsAC , CM000673.1:g.118968305_118968306delinsAC	GRCh37
NC_000011.8:g.118473515_118473516delinsAC	NCBI36
NG_008918.1:g.9480_9481delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-45_976-44delinsGT
ENST00000524658.2:n.957-45_957-44delinsGT
ENST00000530052.2:n.1918_1919delinsGT
ENST00000682191.1:n.1378_1379delinsGT
ENST00000682192.1:n.1120-45_1120-44delinsGT
ENST00000682232.1:c.*622+259_*622+260delinsGT	ENSP00000507302.1:n.*622+259_*622+260delinsGT
ENST00000682326.1:c.917+259_917+260delinsGT	ENSP00000508129.1:n.917+259_917+260delinsGT
ENST00000682404.1:n.2019-45_2019-44delinsGT
ENST00000682517.1:n.2277_2278delinsGT
ENST00000682652.1:n.2147_2148delinsGT
ENST00000682665.1:n.1573_1574delinsGT
ENST00000682691.1:n.1573_1574delinsGT
ENST00000682791.1:c.831-45_831-44delinsGT	ENSP00000507312.1:n.831-45_831-44delinsGT
ENST00000682811.1:c.800-45_800-44delinsGT	ENSP00000508196.1:n.800-45_800-44delinsGT
ENST00000682883.1:n.1032-299_1032-298delinsGT
ENST00000682946.1:c.729-45_729-44delinsGT	ENSP00000506856.1:n.729-45_729-44delinsGT
ENST00000683143.1:c.*623-45_*623-44delinsGT	ENSP00000507168.1:n.*623-45_*623-44delinsGT
ENST00000683373.1:n.1378_1379delinsGT
ENST00000683558.1:n.1378_1379delinsGT
ENST00000683567.1:n.1027-45_1027-44delinsGT
ENST00000683955.1:n.1674-45_1674-44delinsGT
ENST00000684142.1:c.*593-45_*593-44delinsGT	ENSP00000508008.1:n.*593-45_*593-44delinsGT
ENST00000684252.1:n.1315-45_1315-44delinsGT
ENST00000684255.1:c.*623-45_*623-44delinsGT	ENSP00000507398.1:n.*623-45_*623-44delinsGT
ENST00000684315.1:n.1651-45_1651-44delinsGT
ENST00000684345.1:c.*851_*852delinsGT	ENSP00000507163.1:n.*851_*852delinsGT
ENST00000684499.1:c.*1023-45_*1023-44delinsGT	ENSP00000506800.1:n.*1023-45_*1023-44delinsGT
ENST00000684682.1:c.*604_*605delinsGT	ENSP00000507326.1:n.*604_*605delinsGT
ENST00000354202.9:c.918-45_918-44delinsGT MANE Select	ENSP00000346142.4:n.918-45_918-44delinsGT
ENST00000636404.1:c.233-533_233-532delinsGT
ENST00000638850.1:c.422-45_422-44delinsGT
ENST00000639704.1:c.825-45_825-44delinsGT	ENSP00000491336.1:n.825-45_825-44delinsGT
ENST00000640102.1:c.*571-45_*571-44delinsGT	ENSP00000492027.1:n.*571-45_*571-44delinsGT
ENST00000640747.1:c.*593-45_*593-44delinsGT	ENSP00000492730.1:n.*593-45_*593-44delinsGT
ENST00000354202.8:c.918-45_918-44delinsGT	ENSP00000346142.4:n.918-45_918-44delinsGT
ENST00000392834.7:c.*623-45_*623-44delinsGT	ENSP00000376579.3:n.*623-45_*623-44delinsGT
ENST00000409993.6:c.918-45_918-44delinsGT	ENSP00000386597.2:n.918-45_918-44delinsGT
ENST00000414373.5:c.*475-299_*475-298delinsGT	ENSP00000402019.1:n.*475-299_*475-298delinsGT
ENST00000442480.1:c.650-45_650-44delinsGT	ENSP00000406591.1:n.650-45_650-44delinsGT
ENST00000461999.1:n.1040_1041delinsGT
ENST00000481084.5:n.1547-45_1547-44delinsGT
ENST00000524658.1:n.223-45_223-44delinsGT
ENST00000525456.5:n.732-45_732-44delinsGT
NM_001382.3:c.918-45_918-44delinsGT	NP_001373.2:n.918-45_918-44delinsGT
XM_005271422.2:c.918-45_918-44delinsGT	XP_005271479.1:n.918-45_918-44delinsGT
XM_011542648.1:c.597-45_597-44delinsGT	XP_011540950.1:n.597-45_597-44delinsGT
XR_947801.1:n.1165-299_1165-298delinsGT
XM_005271422.3:c.918-45_918-44delinsGT	XP_005271479.1:n.918-45_918-44delinsGT
XM_011542648.2:c.597-45_597-44delinsGT	XP_011540950.1:n.597-45_597-44delinsGT
XM_017017293.2:c.597-45_597-44delinsGT	XP_016872782.1:n.597-45_597-44delinsGT
XM_017017294.2:c.729-45_729-44delinsGT	XP_016872783.1:n.729-45_729-44delinsGT
XM_017017295.1:c.402-45_402-44delinsGT	XP_016872784.1:n.402-45_402-44delinsGT
XR_001747785.2:n.952-45_952-44delinsGT
XR_947801.2:n.952-299_952-298delinsGT
NM_001382.4:c.918-45_918-44delinsGT MANE Select	NP_001373.2:n.918-45_918-44delinsGT