Canonical Allele Identifier: CA602578050

Gene: DPAGT1

Linked Data

• dbSNP Id: rs1179417695
• gnomAD v2: 11-118968124-T-C
• gnomAD v4: 11-119097414-T-C
• MyVariant Identifiers: chr11:g.118968124T>C (hg19) ; chr11:g.119097414T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097414T>C , CM000673.2:g.119097414T>C	GRCh38
NC_000011.9:g.118968124T>C , CM000673.1:g.118968124T>C	GRCh37
NC_000011.8:g.118473334T>C	NCBI36
NG_008918.1:g.9662A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1113A>G
ENST00000524658.2:n.1094A>G
ENST00000530052.2:n.2100A>G
ENST00000682191.1:n.1510+50A>G
ENST00000682192.1:n.1257A>G
ENST00000682232.1:c.*623-117A>G	ENSP00000507302.1:n.*623-117A>G
ENST00000682326.1:c.918-117A>G	ENSP00000508129.1:n.918-117A>G
ENST00000682404.1:n.2156A>G
ENST00000682517.1:n.2459A>G
ENST00000682652.1:n.2279+50A>G
ENST00000682665.1:n.1755A>G
ENST00000682691.1:n.1755A>G
ENST00000682791.1:c.918+50A>G	ENSP00000507312.1:n.918+50A>G
ENST00000682811.1:c.*56+50A>G	ENSP00000508196.1:n.*56+50A>G
ENST00000682883.1:n.1032-117A>G
ENST00000682946.1:c.*87+50A>G	ENSP00000506856.1:n.*87+50A>G
ENST00000683143.1:c.*710+50A>G	ENSP00000507168.1:n.*710+50A>G
ENST00000683373.1:n.1510+50A>G
ENST00000683558.1:n.1560A>G
ENST00000683567.1:n.1114+50A>G
ENST00000683955.1:n.1761+50A>G
ENST00000684142.1:c.*730A>G	ENSP00000508008.1:n.*730A>G
ENST00000684252.1:n.1452A>G
ENST00000684255.1:c.*760A>G	ENSP00000507398.1:n.*760A>G
ENST00000684315.1:n.1738+50A>G
ENST00000684345.1:c.*1033A>G	ENSP00000507163.1:n.*1033A>G
ENST00000684499.1:c.*1160A>G	ENSP00000506800.1:n.*1160A>G
ENST00000684682.1:c.*786A>G	ENSP00000507326.1:n.*786A>G
ENST00000354202.9:c.1005+50A>G MANE Select	ENSP00000346142.4:n.1005+50A>G
ENST00000636404.1:c.233-351A>G
ENST00000638850.1:c.528+31A>G
ENST00000639704.1:c.912+50A>G	ENSP00000491336.1:n.912+50A>G
ENST00000640102.1:c.*658+50A>G	ENSP00000492027.1:n.*658+50A>G
ENST00000640747.1:c.*680+50A>G	ENSP00000492730.1:n.*680+50A>G
ENST00000354202.8:c.1005+50A>G	ENSP00000346142.4:n.1005+50A>G
ENST00000392834.7:c.*710+50A>G	ENSP00000376579.3:n.*710+50A>G
ENST00000409993.6:c.1005+50A>G	ENSP00000386597.2:n.1005+50A>G
ENST00000414373.5:c.*475-117A>G	ENSP00000402019.1:n.*475-117A>G
ENST00000442480.1:c.737+50A>G	ENSP00000406591.1:n.737+50A>G
ENST00000461999.1:n.1222A>G
ENST00000481084.5:n.1634+50A>G
ENST00000524658.1:n.360A>G
ENST00000525456.5:n.869A>G
NM_001382.3:c.1005+50A>G	NP_001373.2:n.1005+50A>G
XM_005271422.2:c.1005+50A>G	XP_005271479.1:n.1005+50A>G
XM_011542648.1:c.684+50A>G	XP_011540950.1:n.684+50A>G
XR_947801.1:n.1165-117A>G
XM_005271422.3:c.1005+50A>G	XP_005271479.1:n.1005+50A>G
XM_011542648.2:c.684+50A>G	XP_011540950.1:n.684+50A>G
XM_017017293.2:c.684+50A>G	XP_016872782.1:n.684+50A>G
XM_017017294.2:c.*137A>G	XP_016872783.1:n.*137A>G
XM_017017295.1:c.489+50A>G	XP_016872784.1:n.489+50A>G
XR_001747785.2:n.1039+50A>G
XR_947801.2:n.952-117A>G
NM_001382.4:c.1005+50A>G MANE Select	NP_001373.2:n.1005+50A>G