Canonical Allele Identifier: CA2003808814

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097447_119097450delinsCCTT , CM000673.2:g.119097447_119097450delinsCCTT	GRCh38
NC_000011.9:g.118968157_118968160delinsCCTT , CM000673.1:g.118968157_118968160delinsCCTT	GRCh37
NC_000011.8:g.118473367_118473370delinsCCTT	NCBI36
NG_008918.1:g.9626_9629delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1077_1080delinsAAGG
ENST00000524658.2:n.1058_1061delinsAAGG
ENST00000530052.2:n.2064_2067delinsAAGG
ENST00000682191.1:n.1510+14_1510+17delinsAAGG
ENST00000682192.1:n.1221_1224delinsAAGG
ENST00000682232.1:c.*623-153_*623-150delinsAAGG	ENSP00000507302.1:n.*623-153_*623-150delinsAAGG
ENST00000682326.1:c.918-153_918-150delinsAAGG	ENSP00000508129.1:n.918-153_918-150delinsAAGG
ENST00000682404.1:n.2120_2123delinsAAGG
ENST00000682517.1:n.2423_2426delinsAAGG
ENST00000682652.1:n.2279+14_2279+17delinsAAGG
ENST00000682665.1:n.1719_1722delinsAAGG
ENST00000682691.1:n.1719_1722delinsAAGG
ENST00000682791.1:c.918+14_918+17delinsAAGG	ENSP00000507312.1:n.918+14_918+17delinsAAGG
ENST00000682811.1:c.*56+14_*56+17delinsAAGG	ENSP00000508196.1:n.*56+14_*56+17delinsAAGG
ENST00000682883.1:n.1032-153_1032-150delinsAAGG
ENST00000682946.1:c.*87+14_*87+17delinsAAGG	ENSP00000506856.1:n.*87+14_*87+17delinsAAGG
ENST00000683143.1:c.*710+14_*710+17delinsAAGG	ENSP00000507168.1:n.*710+14_*710+17delinsAAGG
ENST00000683373.1:n.1510+14_1510+17delinsAAGG
ENST00000683558.1:n.1524_1527delinsAAGG
ENST00000683567.1:n.1114+14_1114+17delinsAAGG
ENST00000683955.1:n.1761+14_1761+17delinsAAGG
ENST00000684142.1:c.*694_*697delinsAAGG	ENSP00000508008.1:n.*694_*697delinsAAGG
ENST00000684252.1:n.1416_1419delinsAAGG
ENST00000684255.1:c.*724_*727delinsAAGG	ENSP00000507398.1:n.*724_*727delinsAAGG
ENST00000684315.1:n.1738+14_1738+17delinsAAGG
ENST00000684345.1:c.*997_*1000delinsAAGG	ENSP00000507163.1:n.*997_*1000delinsAAGG
ENST00000684499.1:c.*1124_*1127delinsAAGG	ENSP00000506800.1:n.*1124_*1127delinsAAGG
ENST00000684682.1:c.*750_*753delinsAAGG	ENSP00000507326.1:n.*750_*753delinsAAGG
ENST00000354202.9:c.1005+14_1005+17delinsAAGG MANE Select	ENSP00000346142.4:n.1005+14_1005+17delinsAAGG
ENST00000636404.1:c.233-387_233-384delinsAAGG
ENST00000638850.1:c.523_526delinsAAGG
ENST00000639704.1:c.912+14_912+17delinsAAGG	ENSP00000491336.1:n.912+14_912+17delinsAAGG
ENST00000640102.1:c.*658+14_*658+17delinsAAGG	ENSP00000492027.1:n.*658+14_*658+17delinsAAGG
ENST00000640747.1:c.*680+14_*680+17delinsAAGG	ENSP00000492730.1:n.*680+14_*680+17delinsAAGG
ENST00000354202.8:c.1005+14_1005+17delinsAAGG	ENSP00000346142.4:n.1005+14_1005+17delinsAAGG
ENST00000392834.7:c.*710+14_*710+17delinsAAGG	ENSP00000376579.3:n.*710+14_*710+17delinsAAGG
ENST00000409993.6:c.1005+14_1005+17delinsAAGG	ENSP00000386597.2:n.1005+14_1005+17delinsAAGG
ENST00000414373.5:c.*475-153_*475-150delinsAAGG	ENSP00000402019.1:n.*475-153_*475-150delinsAAGG
ENST00000442480.1:c.737+14_737+17delinsAAGG	ENSP00000406591.1:n.737+14_737+17delinsAAGG
ENST00000461999.1:n.1186_1189delinsAAGG
ENST00000481084.5:n.1634+14_1634+17delinsAAGG
ENST00000524658.1:n.324_327delinsAAGG
ENST00000525456.5:n.833_836delinsAAGG
NM_001382.3:c.1005+14_1005+17delinsAAGG	NP_001373.2:n.1005+14_1005+17delinsAAGG
XM_005271422.2:c.1005+14_1005+17delinsAAGG	XP_005271479.1:n.1005+14_1005+17delinsAAGG
XM_011542648.1:c.684+14_684+17delinsAAGG	XP_011540950.1:n.684+14_684+17delinsAAGG
XR_947801.1:n.1165-153_1165-150delinsAAGG
XM_005271422.3:c.1005+14_1005+17delinsAAGG	XP_005271479.1:n.1005+14_1005+17delinsAAGG
XM_011542648.2:c.684+14_684+17delinsAAGG	XP_011540950.1:n.684+14_684+17delinsAAGG
XM_017017293.2:c.684+14_684+17delinsAAGG	XP_016872782.1:n.684+14_684+17delinsAAGG
XM_017017294.2:c.*101_*104delinsAAGG	XP_016872783.1:n.*101_*104delinsAAGG
XM_017017295.1:c.489+14_489+17delinsAAGG	XP_016872784.1:n.489+14_489+17delinsAAGG
XR_001747785.2:n.1039+14_1039+17delinsAAGG
XR_947801.2:n.952-153_952-150delinsAAGG
NM_001382.4:c.1005+14_1005+17delinsAAGG MANE Select	NP_001373.2:n.1005+14_1005+17delinsAAGG