Canonical Allele Identifier: CA2616361115

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119097602-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097605del , CM000673.2:g.119097605del	GRCh38
NC_000011.9:g.118968315del , CM000673.1:g.118968315del	GRCh37
NC_000011.8:g.118473525del	NCBI36
NG_008918.1:g.9473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-52del
ENST00000524658.2:n.957-52del
ENST00000530052.2:n.1911del
ENST00000682191.1:n.1371del
ENST00000682192.1:n.1120-52del
ENST00000682232.1:c.*622+252del	ENSP00000507302.1:n.*622+252del
ENST00000682326.1:c.917+252del	ENSP00000508129.1:n.917+252del
ENST00000682404.1:n.2019-52del
ENST00000682517.1:n.2270del
ENST00000682652.1:n.2140del
ENST00000682665.1:n.1566del
ENST00000682691.1:n.1566del
ENST00000682791.1:c.831-52del	ENSP00000507312.1:n.831-52del
ENST00000682811.1:c.800-52del	ENSP00000508196.1:n.800-52del
ENST00000682883.1:n.1032-306del
ENST00000682946.1:c.729-52del	ENSP00000506856.1:n.729-52del
ENST00000683143.1:c.*623-52del	ENSP00000507168.1:n.*623-52del
ENST00000683373.1:n.1371del
ENST00000683558.1:n.1371del
ENST00000683567.1:n.1027-52del
ENST00000683955.1:n.1674-52del
ENST00000684142.1:c.*593-52del	ENSP00000508008.1:n.*593-52del
ENST00000684252.1:n.1315-52del
ENST00000684255.1:c.*623-52del	ENSP00000507398.1:n.*623-52del
ENST00000684315.1:n.1651-52del
ENST00000684345.1:c.*844del	ENSP00000507163.1:n.*844del
ENST00000684499.1:c.*1023-52del	ENSP00000506800.1:n.*1023-52del
ENST00000684682.1:c.*597del	ENSP00000507326.1:n.*597del
ENST00000354202.9:c.918-52del MANE Select	ENSP00000346142.4:n.918-52del
ENST00000636404.1:c.233-540del
ENST00000638850.1:c.422-52del
ENST00000639704.1:c.825-52del	ENSP00000491336.1:n.825-52del
ENST00000640102.1:c.*571-52del	ENSP00000492027.1:n.*571-52del
ENST00000640747.1:c.*593-52del	ENSP00000492730.1:n.*593-52del
ENST00000354202.8:c.918-52del	ENSP00000346142.4:n.918-52del
ENST00000392834.7:c.*623-52del	ENSP00000376579.3:n.*623-52del
ENST00000409993.6:c.918-52del	ENSP00000386597.2:n.918-52del
ENST00000414373.5:c.*475-306del	ENSP00000402019.1:n.*475-306del
ENST00000442480.1:c.650-52del	ENSP00000406591.1:n.650-52del
ENST00000461999.1:n.1033del
ENST00000481084.5:n.1547-52del
ENST00000524658.1:n.223-52del
ENST00000525456.5:n.732-52del
NM_001382.3:c.918-52del	NP_001373.2:n.918-52del
XM_005271422.2:c.918-52del	XP_005271479.1:n.918-52del
XM_011542648.1:c.597-52del	XP_011540950.1:n.597-52del
XR_947801.1:n.1165-306del
XM_005271422.3:c.918-52del	XP_005271479.1:n.918-52del
XM_011542648.2:c.597-52del	XP_011540950.1:n.597-52del
XM_017017293.2:c.597-52del	XP_016872782.1:n.597-52del
XM_017017294.2:c.729-52del	XP_016872783.1:n.729-52del
XM_017017295.1:c.402-52del	XP_016872784.1:n.402-52del
XR_001747785.2:n.952-52del
XR_947801.2:n.952-306del
NM_001382.4:c.918-52del MANE Select	NP_001373.2:n.918-52del