Canonical Allele Identifier: CA382909390

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968176T>C (hg19) ; chr11:g.119097466T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097466T>C , CM000673.2:g.119097466T>C	GRCh38
NC_000011.9:g.118968176T>C , CM000673.1:g.118968176T>C	GRCh37
NC_000011.8:g.118473386T>C	NCBI36
NG_008918.1:g.9610A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1061A>G
ENST00000524658.2:n.1042A>G
ENST00000530052.2:n.2048A>G
ENST00000682191.1:n.1508A>G
ENST00000682192.1:n.1205A>G
ENST00000682232.1:c.*623-169A>G	ENSP00000507302.1:n.*623-169A>G
ENST00000682326.1:c.918-169A>G	ENSP00000508129.1:n.918-169A>G
ENST00000682404.1:n.2104A>G
ENST00000682517.1:n.2407A>G
ENST00000682652.1:n.2277A>G
ENST00000682665.1:n.1703A>G
ENST00000682691.1:n.1703A>G
ENST00000682791.1:c.916A>G	ENSP00000507312.1:p.Lys306Glu
ENST00000682811.1:c.*54A>G	ENSP00000508196.1:n.*54A>G
ENST00000682883.1:n.1032-169A>G
ENST00000682946.1:c.*85A>G	ENSP00000506856.1:n.*85A>G
ENST00000683143.1:c.*708A>G	ENSP00000507168.1:n.*708A>G
ENST00000683373.1:n.1508A>G
ENST00000683558.1:n.1508A>G
ENST00000683567.1:n.1112A>G
ENST00000683955.1:n.1759A>G
ENST00000684142.1:c.*678A>G	ENSP00000508008.1:n.*678A>G
ENST00000684252.1:n.1400A>G
ENST00000684255.1:c.*708A>G	ENSP00000507398.1:n.*708A>G
ENST00000684315.1:n.1736A>G
ENST00000684345.1:c.*981A>G	ENSP00000507163.1:n.*981A>G
ENST00000684499.1:c.*1108A>G	ENSP00000506800.1:n.*1108A>G
ENST00000684682.1:c.*734A>G	ENSP00000507326.1:n.*734A>G
ENST00000354202.9:c.1003A>G MANE Select	ENSP00000346142.4:p.Lys335Glu
ENST00000636404.1:c.233-403A>G
ENST00000638850.1:c.507A>G
ENST00000639704.1:c.910A>G	ENSP00000491336.1:p.Lys304Glu
ENST00000640102.1:c.*656A>G	ENSP00000492027.1:n.*656A>G
ENST00000640747.1:c.*678A>G	ENSP00000492730.1:n.*678A>G
ENST00000354202.8:c.1003A>G	ENSP00000346142.4:p.Lys335Glu
ENST00000392834.7:c.*708A>G	ENSP00000376579.3:n.*708A>G
ENST00000409993.6:c.1003A>G	ENSP00000386597.2:p.Lys335Glu
ENST00000414373.5:c.*475-169A>G	ENSP00000402019.1:n.*475-169A>G
ENST00000442480.1:c.735A>G	ENSP00000406591.1:n.735A>G
ENST00000461999.1:n.1170A>G
ENST00000481084.5:n.1632A>G
ENST00000524658.1:n.308A>G
ENST00000525456.5:n.817A>G
NM_001382.3:c.1003A>G	NP_001373.2:p.Lys335Glu
XM_005271422.2:c.1003A>G	XP_005271479.1:p.Lys335Glu
XM_011542648.1:c.682A>G	XP_011540950.1:p.Lys228Glu
XR_947801.1:n.1165-169A>G
XM_005271422.3:c.1003A>G	XP_005271479.1:p.Lys335Glu
XM_011542648.2:c.682A>G	XP_011540950.1:p.Lys228Glu
XM_017017293.2:c.682A>G	XP_016872782.1:p.Lys228Glu
XM_017017294.2:c.*85A>G	XP_016872783.1:n.*85A>G
XM_017017295.1:c.487A>G	XP_016872784.1:p.Lys163Glu
XR_001747785.2:n.1037A>G
XR_947801.2:n.952-169A>G
NM_001382.4:c.1003A>G MANE Select	NP_001373.2:p.Lys335Glu