Canonical Allele Identifier: CA2616360867

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119097408-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097409del , CM000673.2:g.119097409del	GRCh38
NC_000011.9:g.118968119del , CM000673.1:g.118968119del	GRCh37
NC_000011.8:g.118473329del	NCBI36
NG_008918.1:g.9667del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1118del
ENST00000524658.2:n.1099del
ENST00000530052.2:n.2105del
ENST00000682191.1:n.1510+55del
ENST00000682192.1:n.1262del
ENST00000682232.1:c.*623-112del	ENSP00000507302.1:n.*623-112del
ENST00000682326.1:c.918-112del	ENSP00000508129.1:n.918-112del
ENST00000682404.1:n.2161del
ENST00000682517.1:n.2464del
ENST00000682652.1:n.2279+55del
ENST00000682665.1:n.1760del
ENST00000682691.1:n.1760del
ENST00000682791.1:c.918+55del	ENSP00000507312.1:n.918+55del
ENST00000682811.1:c.*56+55del	ENSP00000508196.1:n.*56+55del
ENST00000682883.1:n.1032-112del
ENST00000682946.1:c.*87+55del	ENSP00000506856.1:n.*87+55del
ENST00000683143.1:c.*710+55del	ENSP00000507168.1:n.*710+55del
ENST00000683373.1:n.1510+55del
ENST00000683558.1:n.1565del
ENST00000683567.1:n.1114+55del
ENST00000683955.1:n.1761+55del
ENST00000684142.1:c.*735del	ENSP00000508008.1:n.*735del
ENST00000684252.1:n.1457del
ENST00000684255.1:c.*765del	ENSP00000507398.1:n.*765del
ENST00000684315.1:n.1738+55del
ENST00000684345.1:c.*1038del	ENSP00000507163.1:n.*1038del
ENST00000684499.1:c.*1165del	ENSP00000506800.1:n.*1165del
ENST00000684682.1:c.*791del	ENSP00000507326.1:n.*791del
ENST00000354202.9:c.1005+55del MANE Select	ENSP00000346142.4:n.1005+55del
ENST00000636404.1:c.233-346del
ENST00000638850.1:c.528+36del
ENST00000639704.1:c.912+55del	ENSP00000491336.1:n.912+55del
ENST00000640102.1:c.*658+55del	ENSP00000492027.1:n.*658+55del
ENST00000640747.1:c.*680+55del	ENSP00000492730.1:n.*680+55del
ENST00000354202.8:c.1005+55del	ENSP00000346142.4:n.1005+55del
ENST00000392834.7:c.*710+55del	ENSP00000376579.3:n.*710+55del
ENST00000409993.6:c.1005+55del	ENSP00000386597.2:n.1005+55del
ENST00000414373.5:c.*475-112del	ENSP00000402019.1:n.*475-112del
ENST00000442480.1:c.737+55del	ENSP00000406591.1:n.737+55del
ENST00000461999.1:n.1227del
ENST00000481084.5:n.1634+55del
ENST00000524658.1:n.365del
ENST00000525456.5:n.874del
NM_001382.3:c.1005+55del	NP_001373.2:n.1005+55del
XM_005271422.2:c.1005+55del	XP_005271479.1:n.1005+55del
XM_011542648.1:c.684+55del	XP_011540950.1:n.684+55del
XR_947801.1:n.1165-112del
XM_005271422.3:c.1005+55del	XP_005271479.1:n.1005+55del
XM_011542648.2:c.684+55del	XP_011540950.1:n.684+55del
XM_017017293.2:c.684+55del	XP_016872782.1:n.684+55del
XM_017017294.2:c.*142del	XP_016872783.1:n.*142del
XM_017017295.1:c.489+55del	XP_016872784.1:n.489+55del
XR_001747785.2:n.1039+55del
XR_947801.2:n.952-112del
NM_001382.4:c.1005+55del MANE Select	NP_001373.2:n.1005+55del