Canonical Allele Identifier: CA2003808882

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097615_119097616delinsTA , CM000673.2:g.119097615_119097616delinsTA	GRCh38
NC_000011.9:g.118968325_118968326delinsTA , CM000673.1:g.118968325_118968326delinsTA	GRCh37
NC_000011.8:g.118473535_118473536delinsTA	NCBI36
NG_008918.1:g.9460_9461delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-65_976-64delinsTA
ENST00000524658.2:n.957-65_957-64delinsTA
ENST00000530052.2:n.1898_1899delinsTA
ENST00000682191.1:n.1358_1359delinsTA
ENST00000682192.1:n.1120-65_1120-64delinsTA
ENST00000682232.1:c.*622+239_*622+240delinsTA	ENSP00000507302.1:n.*622+239_*622+240delinsTA
ENST00000682326.1:c.917+239_917+240delinsTA	ENSP00000508129.1:n.917+239_917+240delinsTA
ENST00000682404.1:n.2019-65_2019-64delinsTA
ENST00000682517.1:n.2257_2258delinsTA
ENST00000682652.1:n.2127_2128delinsTA
ENST00000682665.1:n.1553_1554delinsTA
ENST00000682691.1:n.1553_1554delinsTA
ENST00000682791.1:c.831-65_831-64delinsTA	ENSP00000507312.1:n.831-65_831-64delinsTA
ENST00000682811.1:c.800-65_800-64delinsTA	ENSP00000508196.1:n.800-65_800-64delinsTA
ENST00000682883.1:n.1032-319_1032-318delinsTA
ENST00000682946.1:c.729-65_729-64delinsTA	ENSP00000506856.1:n.729-65_729-64delinsTA
ENST00000683143.1:c.*623-65_*623-64delinsTA	ENSP00000507168.1:n.*623-65_*623-64delinsTA
ENST00000683373.1:n.1358_1359delinsTA
ENST00000683558.1:n.1358_1359delinsTA
ENST00000683567.1:n.1027-65_1027-64delinsTA
ENST00000683955.1:n.1674-65_1674-64delinsTA
ENST00000684142.1:c.*593-65_*593-64delinsTA	ENSP00000508008.1:n.*593-65_*593-64delinsTA
ENST00000684252.1:n.1315-65_1315-64delinsTA
ENST00000684255.1:c.*623-65_*623-64delinsTA	ENSP00000507398.1:n.*623-65_*623-64delinsTA
ENST00000684315.1:n.1651-65_1651-64delinsTA
ENST00000684345.1:c.*831_*832delinsTA	ENSP00000507163.1:n.*831_*832delinsTA
ENST00000684499.1:c.*1023-65_*1023-64delinsTA	ENSP00000506800.1:n.*1023-65_*1023-64delinsTA
ENST00000684682.1:c.*584_*585delinsTA	ENSP00000507326.1:n.*584_*585delinsTA
ENST00000354202.9:c.918-65_918-64delinsTA MANE Select	ENSP00000346142.4:n.918-65_918-64delinsTA
ENST00000636404.1:c.233-553_233-552delinsTA
ENST00000638850.1:c.422-65_422-64delinsTA
ENST00000639704.1:c.825-65_825-64delinsTA	ENSP00000491336.1:n.825-65_825-64delinsTA
ENST00000640102.1:c.*571-65_*571-64delinsTA	ENSP00000492027.1:n.*571-65_*571-64delinsTA
ENST00000640747.1:c.*593-65_*593-64delinsTA	ENSP00000492730.1:n.*593-65_*593-64delinsTA
ENST00000354202.8:c.918-65_918-64delinsTA	ENSP00000346142.4:n.918-65_918-64delinsTA
ENST00000392834.7:c.*623-65_*623-64delinsTA	ENSP00000376579.3:n.*623-65_*623-64delinsTA
ENST00000409993.6:c.918-65_918-64delinsTA	ENSP00000386597.2:n.918-65_918-64delinsTA
ENST00000414373.5:c.*475-319_*475-318delinsTA	ENSP00000402019.1:n.*475-319_*475-318delinsTA
ENST00000442480.1:c.650-65_650-64delinsTA	ENSP00000406591.1:n.650-65_650-64delinsTA
ENST00000461999.1:n.1020_1021delinsTA
ENST00000481084.5:n.1547-65_1547-64delinsTA
ENST00000524658.1:n.223-65_223-64delinsTA
ENST00000525456.5:n.732-65_732-64delinsTA
NM_001382.3:c.918-65_918-64delinsTA	NP_001373.2:n.918-65_918-64delinsTA
XM_005271422.2:c.918-65_918-64delinsTA	XP_005271479.1:n.918-65_918-64delinsTA
XM_011542648.1:c.597-65_597-64delinsTA	XP_011540950.1:n.597-65_597-64delinsTA
XR_947801.1:n.1165-319_1165-318delinsTA
XM_005271422.3:c.918-65_918-64delinsTA	XP_005271479.1:n.918-65_918-64delinsTA
XM_011542648.2:c.597-65_597-64delinsTA	XP_011540950.1:n.597-65_597-64delinsTA
XM_017017293.2:c.597-65_597-64delinsTA	XP_016872782.1:n.597-65_597-64delinsTA
XM_017017294.2:c.729-65_729-64delinsTA	XP_016872783.1:n.729-65_729-64delinsTA
XM_017017295.1:c.402-65_402-64delinsTA	XP_016872784.1:n.402-65_402-64delinsTA
XR_001747785.2:n.952-65_952-64delinsTA
XR_947801.2:n.952-319_952-318delinsTA
NM_001382.4:c.918-65_918-64delinsTA MANE Select	NP_001373.2:n.918-65_918-64delinsTA