Canonical Allele Identifier: CA672381978

Gene: DPAGT1

Linked Data

• dbSNP Id: rs1278799174
• gnomAD v3: 11-119097405-C-T
• gnomAD v4: 11-119097405-C-T
• MyVariant Identifiers: chr11:g.118968115C>T (hg19) ; chr11:g.119097405C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097405C>T , CM000673.2:g.119097405C>T	GRCh38
NC_000011.9:g.118968115C>T , CM000673.1:g.118968115C>T	GRCh37
NC_000011.8:g.118473325C>T	NCBI36
NG_008918.1:g.9671G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1122G>A
ENST00000524658.2:n.1103G>A
ENST00000530052.2:n.2109G>A
ENST00000682191.1:n.1510+59G>A
ENST00000682192.1:n.1266G>A
ENST00000682232.1:c.*623-108G>A	ENSP00000507302.1:n.*623-108G>A
ENST00000682326.1:c.918-108G>A	ENSP00000508129.1:n.918-108G>A
ENST00000682404.1:n.2165G>A
ENST00000682517.1:n.2468G>A
ENST00000682652.1:n.2279+59G>A
ENST00000682665.1:n.1764G>A
ENST00000682691.1:n.1764G>A
ENST00000682791.1:c.918+59G>A	ENSP00000507312.1:n.918+59G>A
ENST00000682811.1:c.*56+59G>A	ENSP00000508196.1:n.*56+59G>A
ENST00000682883.1:n.1032-108G>A
ENST00000682946.1:c.*87+59G>A	ENSP00000506856.1:n.*87+59G>A
ENST00000683143.1:c.*710+59G>A	ENSP00000507168.1:n.*710+59G>A
ENST00000683373.1:n.1510+59G>A
ENST00000683558.1:n.1569G>A
ENST00000683567.1:n.1114+59G>A
ENST00000683955.1:n.1761+59G>A
ENST00000684142.1:c.*739G>A	ENSP00000508008.1:n.*739G>A
ENST00000684252.1:n.1461G>A
ENST00000684255.1:c.*769G>A	ENSP00000507398.1:n.*769G>A
ENST00000684315.1:n.1738+59G>A
ENST00000684345.1:c.*1042G>A	ENSP00000507163.1:n.*1042G>A
ENST00000684499.1:c.*1169G>A	ENSP00000506800.1:n.*1169G>A
ENST00000684682.1:c.*795G>A	ENSP00000507326.1:n.*795G>A
ENST00000354202.9:c.1005+59G>A MANE Select	ENSP00000346142.4:n.1005+59G>A
ENST00000636404.1:c.233-342G>A
ENST00000638850.1:c.528+40G>A
ENST00000639704.1:c.912+59G>A	ENSP00000491336.1:n.912+59G>A
ENST00000640102.1:c.*658+59G>A	ENSP00000492027.1:n.*658+59G>A
ENST00000640747.1:c.*680+59G>A	ENSP00000492730.1:n.*680+59G>A
ENST00000354202.8:c.1005+59G>A	ENSP00000346142.4:n.1005+59G>A
ENST00000392834.7:c.*710+59G>A	ENSP00000376579.3:n.*710+59G>A
ENST00000409993.6:c.1005+59G>A	ENSP00000386597.2:n.1005+59G>A
ENST00000414373.5:c.*475-108G>A	ENSP00000402019.1:n.*475-108G>A
ENST00000442480.1:c.737+59G>A	ENSP00000406591.1:n.737+59G>A
ENST00000461999.1:n.1231G>A
ENST00000481084.5:n.1634+59G>A
ENST00000524658.1:n.369G>A
ENST00000525456.5:n.878G>A
NM_001382.3:c.1005+59G>A	NP_001373.2:n.1005+59G>A
XM_005271422.2:c.1005+59G>A	XP_005271479.1:n.1005+59G>A
XM_011542648.1:c.684+59G>A	XP_011540950.1:n.684+59G>A
XR_947801.1:n.1165-108G>A
XM_005271422.3:c.1005+59G>A	XP_005271479.1:n.1005+59G>A
XM_011542648.2:c.684+59G>A	XP_011540950.1:n.684+59G>A
XM_017017293.2:c.684+59G>A	XP_016872782.1:n.684+59G>A
XM_017017294.2:c.*146G>A	XP_016872783.1:n.*146G>A
XM_017017295.1:c.489+59G>A	XP_016872784.1:n.489+59G>A
XR_001747785.2:n.1039+59G>A
XR_947801.2:n.952-108G>A
NM_001382.4:c.1005+59G>A MANE Select	NP_001373.2:n.1005+59G>A