Canonical Allele Identifier: CA2565271860

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097413dup , CM000673.2:g.119097413dup	GRCh38
NC_000011.9:g.118968123dup , CM000673.1:g.118968123dup	GRCh37
NC_000011.8:g.118473333dup	NCBI36
NG_008918.1:g.9664dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1115dup
ENST00000524658.2:n.1096dup
ENST00000530052.2:n.2102dup
ENST00000682191.1:n.1510+52dup
ENST00000682192.1:n.1259dup
ENST00000682232.1:c.*623-115dup	ENSP00000507302.1:n.*623-115dup
ENST00000682326.1:c.918-115dup	ENSP00000508129.1:n.918-115dup
ENST00000682404.1:n.2158dup
ENST00000682517.1:n.2461dup
ENST00000682652.1:n.2279+52dup
ENST00000682665.1:n.1757dup
ENST00000682691.1:n.1757dup
ENST00000682791.1:c.918+52dup	ENSP00000507312.1:n.918+52dup
ENST00000682811.1:c.*56+52dup	ENSP00000508196.1:n.*56+52dup
ENST00000682883.1:n.1032-115dup
ENST00000682946.1:c.*87+52dup	ENSP00000506856.1:n.*87+52dup
ENST00000683143.1:c.*710+52dup	ENSP00000507168.1:n.*710+52dup
ENST00000683373.1:n.1510+52dup
ENST00000683558.1:n.1562dup
ENST00000683567.1:n.1114+52dup
ENST00000683955.1:n.1761+52dup
ENST00000684142.1:c.*732dup	ENSP00000508008.1:n.*732dup
ENST00000684252.1:n.1454dup
ENST00000684255.1:c.*762dup	ENSP00000507398.1:n.*762dup
ENST00000684315.1:n.1738+52dup
ENST00000684345.1:c.*1035dup	ENSP00000507163.1:n.*1035dup
ENST00000684499.1:c.*1162dup	ENSP00000506800.1:n.*1162dup
ENST00000684682.1:c.*788dup	ENSP00000507326.1:n.*788dup
ENST00000354202.9:c.1005+52dup MANE Select	ENSP00000346142.4:n.1005+52dup
ENST00000636404.1:c.233-349dup
ENST00000638850.1:c.528+33dup
ENST00000639704.1:c.912+52dup	ENSP00000491336.1:n.912+52dup
ENST00000640102.1:c.*658+52dup	ENSP00000492027.1:n.*658+52dup
ENST00000640747.1:c.*680+52dup	ENSP00000492730.1:n.*680+52dup
ENST00000354202.8:c.1005+52dup	ENSP00000346142.4:n.1005+52dup
ENST00000392834.7:c.*710+52dup	ENSP00000376579.3:n.*710+52dup
ENST00000409993.6:c.1005+52dup	ENSP00000386597.2:n.1005+52dup
ENST00000414373.5:c.*475-115dup	ENSP00000402019.1:n.*475-115dup
ENST00000442480.1:c.737+52dup	ENSP00000406591.1:n.737+52dup
ENST00000461999.1:n.1224dup
ENST00000481084.5:n.1634+52dup
ENST00000524658.1:n.362dup
ENST00000525456.5:n.871dup
NM_001382.3:c.1005+52dup	NP_001373.2:n.1005+52dup
XM_005271422.2:c.1005+52dup	XP_005271479.1:n.1005+52dup
XM_011542648.1:c.684+52dup	XP_011540950.1:n.684+52dup
XR_947801.1:n.1165-115dup
XM_005271422.3:c.1005+52dup	XP_005271479.1:n.1005+52dup
XM_011542648.2:c.684+52dup	XP_011540950.1:n.684+52dup
XM_017017293.2:c.684+52dup	XP_016872782.1:n.684+52dup
XM_017017294.2:c.*139dup	XP_016872783.1:n.*139dup
XM_017017295.1:c.489+52dup	XP_016872784.1:n.489+52dup
XR_001747785.2:n.1039+52dup
XR_947801.2:n.952-115dup
NM_001382.4:c.1005+52dup MANE Select	NP_001373.2:n.1005+52dup