Canonical Allele Identifier: CA382909467

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968184A>C (hg19) ; chr11:g.119097474A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097474A>C , CM000673.2:g.119097474A>C	GRCh38
NC_000011.9:g.118968184A>C , CM000673.1:g.118968184A>C	GRCh37
NC_000011.8:g.118473394A>C	NCBI36
NG_008918.1:g.9602T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1053T>G
ENST00000524658.2:n.1034T>G
ENST00000530052.2:n.2040T>G
ENST00000682191.1:n.1500T>G
ENST00000682192.1:n.1197T>G
ENST00000682232.1:c.*623-177T>G	ENSP00000507302.1:n.*623-177T>G
ENST00000682326.1:c.918-177T>G	ENSP00000508129.1:n.918-177T>G
ENST00000682404.1:n.2096T>G
ENST00000682517.1:n.2399T>G
ENST00000682652.1:n.2269T>G
ENST00000682665.1:n.1695T>G
ENST00000682691.1:n.1695T>G
ENST00000682791.1:c.908T>G	ENSP00000507312.1:p.Phe303Cys
ENST00000682811.1:c.*46T>G	ENSP00000508196.1:n.*46T>G
ENST00000682883.1:n.1032-177T>G
ENST00000682946.1:c.*77T>G	ENSP00000506856.1:n.*77T>G
ENST00000683143.1:c.*700T>G	ENSP00000507168.1:n.*700T>G
ENST00000683373.1:n.1500T>G
ENST00000683558.1:n.1500T>G
ENST00000683567.1:n.1104T>G
ENST00000683955.1:n.1751T>G
ENST00000684142.1:c.*670T>G	ENSP00000508008.1:n.*670T>G
ENST00000684252.1:n.1392T>G
ENST00000684255.1:c.*700T>G	ENSP00000507398.1:n.*700T>G
ENST00000684315.1:n.1728T>G
ENST00000684345.1:c.*973T>G	ENSP00000507163.1:n.*973T>G
ENST00000684499.1:c.*1100T>G	ENSP00000506800.1:n.*1100T>G
ENST00000684682.1:c.*726T>G	ENSP00000507326.1:n.*726T>G
ENST00000354202.9:c.995T>G MANE Select	ENSP00000346142.4:p.Phe332Cys
ENST00000636404.1:c.233-411T>G
ENST00000638850.1:c.499T>G
ENST00000639704.1:c.902T>G	ENSP00000491336.1:p.Phe301Cys
ENST00000640102.1:c.*648T>G	ENSP00000492027.1:n.*648T>G
ENST00000640747.1:c.*670T>G	ENSP00000492730.1:n.*670T>G
ENST00000354202.8:c.995T>G	ENSP00000346142.4:p.Phe332Cys
ENST00000392834.7:c.*700T>G	ENSP00000376579.3:n.*700T>G
ENST00000409993.6:c.995T>G	ENSP00000386597.2:p.Phe332Cys
ENST00000414373.5:c.*475-177T>G	ENSP00000402019.1:n.*475-177T>G
ENST00000442480.1:c.727T>G	ENSP00000406591.1:n.727T>G
ENST00000461999.1:n.1162T>G
ENST00000481084.5:n.1624T>G
ENST00000524658.1:n.300T>G
ENST00000525456.5:n.809T>G
NM_001382.3:c.995T>G	NP_001373.2:p.Phe332Cys
XM_005271422.2:c.995T>G	XP_005271479.1:p.Phe332Cys
XM_011542648.1:c.674T>G	XP_011540950.1:p.Phe225Cys
XR_947801.1:n.1165-177T>G
XM_005271422.3:c.995T>G	XP_005271479.1:p.Phe332Cys
XM_011542648.2:c.674T>G	XP_011540950.1:p.Phe225Cys
XM_017017293.2:c.674T>G	XP_016872782.1:p.Phe225Cys
XM_017017294.2:c.*77T>G	XP_016872783.1:n.*77T>G
XM_017017295.1:c.479T>G	XP_016872784.1:p.Phe160Cys
XR_001747785.2:n.1029T>G
XR_947801.2:n.952-177T>G
NM_001382.4:c.995T>G MANE Select	NP_001373.2:p.Phe332Cys