Canonical Allele Identifier: CA2366211148
Gene: PIGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45424229C= , CM000682.2:g.45424229C= GRCh38
NC_000020.10:g.44052869C= , CM000682.1:g.44052869C= GRCh37
NC_000020.9:g.43486283C= NCBI36
NG_047154.1:g.13163C=

Transcript Alleles

HGVS Amino-acid change
ENST00000424705.3:c.1248C= ENSP00000491856.2:p.Tyr416=
ENST00000638691.2:c.1248C= ENSP00000492094.2:p.Tyr416=
ENST00000639292.2:c.1329C= ENSP00000491678.2:p.Tyr443=
ENST00000640549.2:c.1248C= ENSP00000492043.2:p.Tyr416=
ENST00000687237.1:n.638C=
ENST00000689203.1:c.1248C= ENSP00000508682.1:p.Tyr416=
ENST00000690879.1:n.724C=
ENST00000692236.1:c.1248C= ENSP00000509421.1:p.Tyr416=
ENST00000279035.14:c.942C= ENSP00000279035.8:p.Tyr314=
ENST00000279036.12:c.1248C= MANE Select ENSP00000279036.6:p.Tyr416=
ENST00000432270.2:c.741C= ENSP00000408354.2:p.Tyr247=
ENST00000543458.7:c.1080C= ENSP00000441577.1:p.Tyr360=
ENST00000545755.3:c.666C= ENSP00000443963.3:p.Tyr222=
ENST00000638241.1:n.1126C=
ENST00000638246.1:c.*748C= ENSP00000492883.1:n.*748C=
ENST00000638277.1:c.182C=
ENST00000638383.1:c.*597C= ENSP00000492295.1:n.*597C=
ENST00000638387.1:c.*292C= ENSP00000492873.1:n.*292C=
ENST00000638415.1:c.785C=
ENST00000638445.1:c.*632C= ENSP00000491297.1:n.*632C=
ENST00000638537.1:n.1037C=
ENST00000638594.1:c.1248C= ENSP00000491697.1:p.Tyr416=
ENST00000638612.1:c.1248C= ENSP00000491458.1:p.Tyr416=
ENST00000638671.1:c.*632C= ENSP00000492875.1:n.*632C=
ENST00000638689.1:n.3455C=
ENST00000638691.1:c.5C=
ENST00000638710.1:c.1454C= ENSP00000491406.1:n.1454C=
ENST00000638714.1:c.*632C= ENSP00000491194.1:n.*632C=
ENST00000638745.1:c.*632C= ENSP00000491744.1:n.*632C=
ENST00000638927.1:c.390C= ENSP00000492335.1:p.Tyr130=
ENST00000638938.1:c.*704C= ENSP00000491171.1:n.*704C=
ENST00000638962.1:n.1208C=
ENST00000638978.1:c.1198C= ENSP00000492743.1:p.Pro400=
ENST00000639250.1:n.2498C=
ENST00000639292.1:c.1108C=
ENST00000639382.1:c.1107C= ENSP00000491534.1:p.Tyr369=
ENST00000639417.1:c.*292C= ENSP00000491058.1:n.*292C=
ENST00000639499.1:c.1248C= ENSP00000491170.1:p.Tyr416=
ENST00000639664.1:n.975C=
ENST00000639783.1:c.*550C= ENSP00000491772.1:n.*550C=
ENST00000639872.1:n.817C=
ENST00000639932.1:c.*550C= ENSP00000491600.1:n.*550C=
ENST00000639984.1:c.*550C= ENSP00000492727.1:n.*550C=
ENST00000640107.1:c.*508C= ENSP00000491118.1:n.*508C=
ENST00000640108.1:c.*937C= ENSP00000492007.1:n.*937C=
ENST00000640175.1:c.*550C= ENSP00000492418.1:n.*550C=
ENST00000640194.1:c.*567C= ENSP00000492279.1:n.*567C=
ENST00000640210.1:c.837C= ENSP00000491164.1:p.Tyr279=
ENST00000640253.1:n.462C=
ENST00000640272.1:c.*632C= ENSP00000492270.1:n.*632C=
ENST00000640324.1:c.1254C= ENSP00000491074.1:p.Tyr418=
ENST00000640364.1:n.1971C=
ENST00000640542.1:c.1047C= ENSP00000492174.1:p.Tyr349=
ENST00000640549.1:c.738C= ENSP00000492043.1:p.Tyr246=
ENST00000640585.1:c.*905C= ENSP00000491308.1:n.*905C=
ENST00000640638.1:n.416C=
ENST00000640666.1:c.1248C= ENSP00000491072.1:p.Tyr416=
ENST00000640692.1:c.*164C= ENSP00000492370.1:n.*164C=
ENST00000640940.1:n.910C=
ENST00000640986.1:c.*365C= ENSP00000491886.1:n.*365C=
ENST00000640996.1:c.*925C= ENSP00000492464.1:n.*925C=
ENST00000279035.13:c.942C= ENSP00000279035.8:p.Tyr314=
ENST00000279036.10:c.1248C= ENSP00000279036.6:p.Tyr416=
ENST00000372689.9:c.1047C= ENSP00000361774.4:p.Tyr349=
ENST00000455050.2:c.*779C= ENSP00000407574.2:n.*779C=
ENST00000543458.6:c.1080C= ENSP00000441577.1:p.Tyr360=
ENST00000545755.2:c.277C=
NM_001184728.2:c.1080C= NP_001171657.1:p.Tyr360=
NM_001184729.2:c.1047C= NP_001171658.1:p.Tyr349=
NM_001184730.2:c.942C= NP_001171659.1:p.Tyr314=
NM_015937.5:c.1248C= NP_057021.2:p.Tyr416=
NR_047691.1:n.1298C=
NR_047692.1:n.1241C=
NR_047693.1:n.1237C=
NR_047694.1:n.1160C=
NR_047695.1:n.931C=
XM_005260430.2:c.741C= XP_005260487.1:p.Tyr247=
XM_005260432.1:c.462C= XP_005260489.1:p.Tyr154=
XM_005260432.3:c.462C= XP_005260489.1:p.Tyr154=
XR_001754286.2:n.1284C=
XR_001754287.2:n.1083C=
NM_015937.6:c.1248C= MANE Select NP_057021.2:p.Tyr416=
NM_001184728.3:c.1080C= NP_001171657.1:p.Tyr360=
NM_001184729.3:c.1047C= NP_001171658.1:p.Tyr349=
NM_001184730.3:c.942C= NP_001171659.1:p.Tyr314=
NR_047691.2:n.1224C=
NR_047692.2:n.1167C=
NR_047693.2:n.1163C=
NR_047694.2:n.1086C=
NR_047695.2:n.857C=