Canonical Allele Identifier: CA2003808896

Gene: DPAGT1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097650_119097652delinsCTA , CM000673.2:g.119097650_119097652delinsCTA	GRCh38
NC_000011.9:g.118968360_118968362delinsCTA , CM000673.1:g.118968360_118968362delinsCTA	GRCh37
NC_000011.8:g.118473570_118473572delinsCTA	NCBI36
NG_008918.1:g.9424_9426delinsTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-101_976-99delinsTAG
ENST00000524658.2:n.957-101_957-99delinsTAG
ENST00000530052.2:n.1862_1864delinsTAG
ENST00000682191.1:n.1322_1324delinsTAG
ENST00000682192.1:n.1120-101_1120-99delinsTAG
ENST00000682232.1:c.*622+203_*622+205delinsTAG	ENSP00000507302.1:n.*622+203_*622+205delinsTAG
ENST00000682326.1:c.917+203_917+205delinsTAG	ENSP00000508129.1:n.917+203_917+205delinsTAG
ENST00000682404.1:n.2019-101_2019-99delinsTAG
ENST00000682517.1:n.2221_2223delinsTAG
ENST00000682652.1:n.2091_2093delinsTAG
ENST00000682665.1:n.1517_1519delinsTAG
ENST00000682691.1:n.1517_1519delinsTAG
ENST00000682791.1:c.831-101_831-99delinsTAG	ENSP00000507312.1:n.831-101_831-99delinsTAG
ENST00000682811.1:c.800-101_800-99delinsTAG	ENSP00000508196.1:n.800-101_800-99delinsTAG
ENST00000682883.1:n.1032-355_1032-353delinsTAG
ENST00000682946.1:c.729-101_729-99delinsTAG	ENSP00000506856.1:n.729-101_729-99delinsTAG
ENST00000683143.1:c.*623-101_*623-99delinsTAG	ENSP00000507168.1:n.*623-101_*623-99delinsTAG
ENST00000683373.1:n.1322_1324delinsTAG
ENST00000683558.1:n.1322_1324delinsTAG
ENST00000683567.1:n.1027-101_1027-99delinsTAG
ENST00000683955.1:n.1674-101_1674-99delinsTAG
ENST00000684142.1:c.*593-101_*593-99delinsTAG	ENSP00000508008.1:n.*593-101_*593-99delinsTAG
ENST00000684252.1:n.1315-101_1315-99delinsTAG
ENST00000684255.1:c.*623-101_*623-99delinsTAG	ENSP00000507398.1:n.*623-101_*623-99delinsTAG
ENST00000684315.1:n.1651-101_1651-99delinsTAG
ENST00000684345.1:c.*795_*797delinsTAG	ENSP00000507163.1:n.*795_*797delinsTAG
ENST00000684499.1:c.*1023-101_*1023-99delinsTAG	ENSP00000506800.1:n.*1023-101_*1023-99delinsTAG
ENST00000684682.1:c.*548_*550delinsTAG	ENSP00000507326.1:n.*548_*550delinsTAG
ENST00000354202.9:c.918-101_918-99delinsTAG MANE Select	ENSP00000346142.4:n.918-101_918-99delinsTAG
ENST00000636404.1:c.233-589_233-587delinsTAG
ENST00000638850.1:c.422-101_422-99delinsTAG
ENST00000639704.1:c.825-101_825-99delinsTAG	ENSP00000491336.1:n.825-101_825-99delinsTAG
ENST00000640102.1:c.*571-101_*571-99delinsTAG	ENSP00000492027.1:n.*571-101_*571-99delinsTAG
ENST00000640747.1:c.*593-101_*593-99delinsTAG	ENSP00000492730.1:n.*593-101_*593-99delinsTAG
ENST00000354202.8:c.918-101_918-99delinsTAG	ENSP00000346142.4:n.918-101_918-99delinsTAG
ENST00000392834.7:c.*623-101_*623-99delinsTAG	ENSP00000376579.3:n.*623-101_*623-99delinsTAG
ENST00000409993.6:c.918-101_918-99delinsTAG	ENSP00000386597.2:n.918-101_918-99delinsTAG
ENST00000414373.5:c.*475-355_*475-353delinsTAG	ENSP00000402019.1:n.*475-355_*475-353delinsTAG
ENST00000442480.1:c.650-101_650-99delinsTAG	ENSP00000406591.1:n.650-101_650-99delinsTAG
ENST00000461999.1:n.984_986delinsTAG
ENST00000481084.5:n.1547-101_1547-99delinsTAG
ENST00000524658.1:n.223-101_223-99delinsTAG
ENST00000525456.5:n.732-101_732-99delinsTAG
NM_001382.3:c.918-101_918-99delinsTAG	NP_001373.2:n.918-101_918-99delinsTAG
XM_005271422.2:c.918-101_918-99delinsTAG	XP_005271479.1:n.918-101_918-99delinsTAG
XM_011542648.1:c.597-101_597-99delinsTAG	XP_011540950.1:n.597-101_597-99delinsTAG
XR_947801.1:n.1165-355_1165-353delinsTAG
XM_005271422.3:c.918-101_918-99delinsTAG	XP_005271479.1:n.918-101_918-99delinsTAG
XM_011542648.2:c.597-101_597-99delinsTAG	XP_011540950.1:n.597-101_597-99delinsTAG
XM_017017293.2:c.597-101_597-99delinsTAG	XP_016872782.1:n.597-101_597-99delinsTAG
XM_017017294.2:c.729-101_729-99delinsTAG	XP_016872783.1:n.729-101_729-99delinsTAG
XM_017017295.1:c.402-101_402-99delinsTAG	XP_016872784.1:n.402-101_402-99delinsTAG
XR_001747785.2:n.952-101_952-99delinsTAG
XR_947801.2:n.952-355_952-353delinsTAG
NM_001382.4:c.918-101_918-99delinsTAG MANE Select	NP_001373.2:n.918-101_918-99delinsTAG