Canonical Allele Identifier: CA2616360934

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119097512-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097513_119097514del , CM000673.2:g.119097513_119097514del	GRCh38
NC_000011.9:g.118968223_118968224del , CM000673.1:g.118968223_118968224del	GRCh37
NC_000011.8:g.118473433_118473434del	NCBI36
NG_008918.1:g.9562_9563del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1013_1014del
ENST00000524658.2:n.994_995del
ENST00000530052.2:n.2000_2001del
ENST00000682191.1:n.1460_1461del
ENST00000682192.1:n.1157_1158del
ENST00000682232.1:c.*623-217_*623-216del	ENSP00000507302.1:n.*623-217_*623-216del
ENST00000682326.1:c.918-217_918-216del	ENSP00000508129.1:n.918-217_918-216del
ENST00000682404.1:n.2056_2057del
ENST00000682517.1:n.2359_2360del
ENST00000682652.1:n.2229_2230del
ENST00000682665.1:n.1655_1656del
ENST00000682691.1:n.1655_1656del
ENST00000682791.1:c.868_869del	ENSP00000507312.1:p.Ser290GlnfsTer30
ENST00000682811.1:c.*6_*7del	ENSP00000508196.1:n.*6_*7del
ENST00000682883.1:n.1032-217_1032-216del
ENST00000682946.1:c.*37_*38del	ENSP00000506856.1:n.*37_*38del
ENST00000683143.1:c.*660_*661del	ENSP00000507168.1:n.*660_*661del
ENST00000683373.1:n.1460_1461del
ENST00000683558.1:n.1460_1461del
ENST00000683567.1:n.1064_1065del
ENST00000683955.1:n.1711_1712del
ENST00000684142.1:c.*630_*631del	ENSP00000508008.1:n.*630_*631del
ENST00000684252.1:n.1352_1353del
ENST00000684255.1:c.*660_*661del	ENSP00000507398.1:n.*660_*661del
ENST00000684315.1:n.1688_1689del
ENST00000684345.1:c.*933_*934del	ENSP00000507163.1:n.*933_*934del
ENST00000684499.1:c.*1060_*1061del	ENSP00000506800.1:n.*1060_*1061del
ENST00000684682.1:c.*686_*687del	ENSP00000507326.1:n.*686_*687del
ENST00000354202.9:c.955_956del MANE Select	ENSP00000346142.4:p.Ser319GlnfsTer30
ENST00000636404.1:c.233-451_233-450del
ENST00000638850.1:c.459_460del
ENST00000639704.1:c.862_863del	ENSP00000491336.1:p.Ser288GlnfsTer30
ENST00000640102.1:c.*608_*609del	ENSP00000492027.1:n.*608_*609del
ENST00000640747.1:c.*630_*631del	ENSP00000492730.1:n.*630_*631del
ENST00000354202.8:c.955_956del	ENSP00000346142.4:p.Ser319GlnfsTer30
ENST00000392834.7:c.*660_*661del	ENSP00000376579.3:n.*660_*661del
ENST00000409993.6:c.955_956del	ENSP00000386597.2:p.Ser319GlnfsTer30
ENST00000414373.5:c.*475-217_*475-216del	ENSP00000402019.1:n.*475-217_*475-216del
ENST00000442480.1:c.687_688del	ENSP00000406591.1:n.687_688del
ENST00000461999.1:n.1122_1123del
ENST00000481084.5:n.1584_1585del
ENST00000524658.1:n.260_261del
ENST00000525456.5:n.769_770del
NM_001382.3:c.955_956del	NP_001373.2:p.Ser319GlnfsTer30
XM_005271422.2:c.955_956del	XP_005271479.1:p.Ser319GlnfsTer30
XM_011542648.1:c.634_635del	XP_011540950.1:p.Ser212GlnfsTer30
XR_947801.1:n.1165-217_1165-216del
XM_005271422.3:c.955_956del	XP_005271479.1:p.Ser319GlnfsTer30
XM_011542648.2:c.634_635del	XP_011540950.1:p.Ser212GlnfsTer30
XM_017017293.2:c.634_635del	XP_016872782.1:p.Ser212GlnfsTer30
XM_017017294.2:c.*37_*38del	XP_016872783.1:n.*37_*38del
XM_017017295.1:c.439_440del	XP_016872784.1:p.Ser147GlnfsTer30
XR_001747785.2:n.989_990del
XR_947801.2:n.952-217_952-216del
NM_001382.4:c.955_956del MANE Select	NP_001373.2:p.Ser319GlnfsTer30