Canonical Allele Identifier: CA382914844

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118971110A>C (hg19) ; chr11:g.119100400A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100400A>C , CM000673.2:g.119100400A>C	GRCh38
NC_000011.9:g.118971110A>C , CM000673.1:g.118971110A>C	GRCh37
NC_000011.8:g.118476320A>C	NCBI36
NG_008918.1:g.6676T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.681T>G
ENST00000530052.2:n.1247T>G
ENST00000682191.1:n.707T>G
ENST00000682192.1:n.707T>G
ENST00000682232.1:c.*210T>G	ENSP00000507302.1:n.*210T>G
ENST00000682326.1:c.505T>G	ENSP00000508129.1:p.Tyr169Asp
ENST00000682404.1:n.1247T>G
ENST00000682517.1:n.1247T>G
ENST00000682652.1:n.1476T>G
ENST00000682665.1:n.902T>G
ENST00000682691.1:n.902T>G
ENST00000682791.1:c.418T>G	ENSP00000507312.1:p.Tyr140Asp
ENST00000682811.1:c.505T>G	ENSP00000508196.1:p.Tyr169Asp
ENST00000682883.1:n.808T>G
ENST00000682946.1:c.505T>G	ENSP00000506856.1:p.Tyr169Asp
ENST00000683143.1:c.*210T>G	ENSP00000507168.1:n.*210T>G
ENST00000683373.1:n.707T>G
ENST00000683558.1:n.707T>G
ENST00000683567.1:n.732T>G
ENST00000683955.1:n.902T>G
ENST00000684142.1:c.*180T>G	ENSP00000508008.1:n.*180T>G
ENST00000684252.1:n.902T>G
ENST00000684255.1:c.*210T>G	ENSP00000507398.1:n.*210T>G
ENST00000684315.1:n.1238T>G
ENST00000684345.1:c.*180T>G	ENSP00000507163.1:n.*180T>G
ENST00000684499.1:c.*610T>G	ENSP00000506800.1:n.*610T>G
ENST00000684682.1:c.170T>G	ENSP00000507326.1:p.Val57Gly
ENST00000354202.9:c.505T>G MANE Select	ENSP00000346142.4:p.Tyr169Asp
ENST00000636404.1:c.9T>G
ENST00000638850.1:c.9T>G
ENST00000639704.1:c.412T>G	ENSP00000491336.1:p.Tyr138Asp
ENST00000640102.1:c.*158T>G	ENSP00000492027.1:n.*158T>G
ENST00000640747.1:c.*180T>G	ENSP00000492730.1:n.*180T>G
ENST00000354202.8:c.505T>G	ENSP00000346142.4:p.Tyr169Asp
ENST00000392834.7:c.*210T>G	ENSP00000376579.3:n.*210T>G
ENST00000409993.6:c.505T>G	ENSP00000386597.2:p.Tyr169Asp
ENST00000414373.5:c.*251T>G	ENSP00000402019.1:n.*251T>G
ENST00000442480.1:c.355T>G	ENSP00000406591.1:p.Tyr119Asp
ENST00000461999.1:n.10T>G
ENST00000481084.5:n.1134T>G
ENST00000525456.5:n.508T>G
ENST00000530052.1:n.403T>G
ENST00000533687.1:n.517T>G
NM_001382.3:c.505T>G	NP_001373.2:p.Tyr169Asp
XM_005271422.2:c.505T>G	XP_005271479.1:p.Tyr169Asp
XM_011542648.1:c.184T>G	XP_011540950.1:p.Tyr62Asp
XR_947801.1:n.941T>G
XM_005271422.3:c.505T>G	XP_005271479.1:p.Tyr169Asp
XM_011542648.2:c.184T>G	XP_011540950.1:p.Tyr62Asp
XM_017017293.2:c.184T>G	XP_016872782.1:p.Tyr62Asp
XM_017017294.2:c.505T>G	XP_016872783.1:p.Tyr169Asp
XM_017017295.1:c.-12T>G	XP_016872784.1:n.-12T>G
XR_001747785.2:n.728T>G
XR_947801.2:n.728T>G
NM_001382.4:c.505T>G MANE Select	NP_001373.2:p.Tyr169Asp