Canonical Allele Identifier: CA2366211151
Gene: PIGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45424233C= , CM000682.2:g.45424233C= GRCh38
NC_000020.10:g.44052873C= , CM000682.1:g.44052873C= GRCh37
NC_000020.9:g.43486287C= NCBI36
NG_047154.1:g.13167C=

Transcript Alleles

HGVS Amino-acid change
ENST00000424705.3:c.1252C= ENSP00000491856.2:p.Pro418=
ENST00000638691.2:c.1252C= ENSP00000492094.2:p.Pro418=
ENST00000639292.2:c.1333C= ENSP00000491678.2:p.Pro445=
ENST00000640549.2:c.1252C= ENSP00000492043.2:p.Pro418=
ENST00000687237.1:n.642C=
ENST00000689203.1:c.1252C= ENSP00000508682.1:p.Pro418=
ENST00000690879.1:n.728C=
ENST00000692236.1:c.1252C= ENSP00000509421.1:p.Pro418=
ENST00000279035.14:c.946C= ENSP00000279035.8:p.Pro316=
ENST00000279036.12:c.1252C= MANE Select ENSP00000279036.6:p.Pro418=
ENST00000432270.2:c.745C= ENSP00000408354.2:p.Pro249=
ENST00000543458.7:c.1084C= ENSP00000441577.1:p.Pro362=
ENST00000545755.3:c.670C= ENSP00000443963.3:p.Pro224=
ENST00000638241.1:n.1130C=
ENST00000638246.1:c.*752C= ENSP00000492883.1:n.*752C=
ENST00000638277.1:c.186C=
ENST00000638383.1:c.*601C= ENSP00000492295.1:n.*601C=
ENST00000638387.1:c.*296C= ENSP00000492873.1:n.*296C=
ENST00000638415.1:c.789C=
ENST00000638445.1:c.*636C= ENSP00000491297.1:n.*636C=
ENST00000638537.1:n.1041C=
ENST00000638594.1:c.1252C= ENSP00000491697.1:p.Pro418=
ENST00000638612.1:c.1252C= ENSP00000491458.1:p.Pro418=
ENST00000638671.1:c.*636C= ENSP00000492875.1:n.*636C=
ENST00000638689.1:n.3459C=
ENST00000638691.1:c.9C=
ENST00000638710.1:c.1458C= ENSP00000491406.1:n.1458C=
ENST00000638714.1:c.*636C= ENSP00000491194.1:n.*636C=
ENST00000638745.1:c.*636C= ENSP00000491744.1:n.*636C=
ENST00000638927.1:c.394C= ENSP00000492335.1:p.Pro132=
ENST00000638938.1:c.*708C= ENSP00000491171.1:n.*708C=
ENST00000638962.1:n.1212C=
ENST00000638978.1:c.1202C= ENSP00000492743.1:p.Ala401=
ENST00000639250.1:n.2502C=
ENST00000639292.1:c.1112C=
ENST00000639382.1:c.1111C= ENSP00000491534.1:p.Pro371=
ENST00000639417.1:c.*296C= ENSP00000491058.1:n.*296C=
ENST00000639499.1:c.1252C= ENSP00000491170.1:p.Pro418=
ENST00000639664.1:n.979C=
ENST00000639783.1:c.*554C= ENSP00000491772.1:n.*554C=
ENST00000639872.1:n.821C=
ENST00000639932.1:c.*554C= ENSP00000491600.1:n.*554C=
ENST00000639984.1:c.*554C= ENSP00000492727.1:n.*554C=
ENST00000640107.1:c.*512C= ENSP00000491118.1:n.*512C=
ENST00000640108.1:c.*941C= ENSP00000492007.1:n.*941C=
ENST00000640175.1:c.*554C= ENSP00000492418.1:n.*554C=
ENST00000640194.1:c.*571C= ENSP00000492279.1:n.*571C=
ENST00000640210.1:c.841C= ENSP00000491164.1:p.Pro281=
ENST00000640253.1:n.466C=
ENST00000640272.1:c.*636C= ENSP00000492270.1:n.*636C=
ENST00000640324.1:c.1258C= ENSP00000491074.1:p.Pro420=
ENST00000640364.1:n.1975C=
ENST00000640542.1:c.1051C= ENSP00000492174.1:p.Pro351=
ENST00000640549.1:c.742C= ENSP00000492043.1:p.Pro248=
ENST00000640585.1:c.*909C= ENSP00000491308.1:n.*909C=
ENST00000640638.1:n.420C=
ENST00000640666.1:c.1252C= ENSP00000491072.1:p.Pro418=
ENST00000640692.1:c.*168C= ENSP00000492370.1:n.*168C=
ENST00000640940.1:n.914C=
ENST00000640986.1:c.*369C= ENSP00000491886.1:n.*369C=
ENST00000640996.1:c.*929C= ENSP00000492464.1:n.*929C=
ENST00000279035.13:c.946C= ENSP00000279035.8:p.Pro316=
ENST00000279036.10:c.1252C= ENSP00000279036.6:p.Pro418=
ENST00000372689.9:c.1051C= ENSP00000361774.4:p.Pro351=
ENST00000455050.2:c.*783C= ENSP00000407574.2:n.*783C=
ENST00000543458.6:c.1084C= ENSP00000441577.1:p.Pro362=
ENST00000545755.2:c.281C=
NM_001184728.2:c.1084C= NP_001171657.1:p.Pro362=
NM_001184729.2:c.1051C= NP_001171658.1:p.Pro351=
NM_001184730.2:c.946C= NP_001171659.1:p.Pro316=
NM_015937.5:c.1252C= NP_057021.2:p.Pro418=
NR_047691.1:n.1302C=
NR_047692.1:n.1245C=
NR_047693.1:n.1241C=
NR_047694.1:n.1164C=
NR_047695.1:n.935C=
XM_005260430.2:c.745C= XP_005260487.1:p.Pro249=
XM_005260432.1:c.466C= XP_005260489.1:p.Pro156=
XM_005260432.3:c.466C= XP_005260489.1:p.Pro156=
XR_001754286.2:n.1288C=
XR_001754287.2:n.1087C=
NM_015937.6:c.1252C= MANE Select NP_057021.2:p.Pro418=
NM_001184728.3:c.1084C= NP_001171657.1:p.Pro362=
NM_001184729.3:c.1051C= NP_001171658.1:p.Pro351=
NM_001184730.3:c.946C= NP_001171659.1:p.Pro316=
NR_047691.2:n.1228C=
NR_047692.2:n.1171C=
NR_047693.2:n.1167C=
NR_047694.2:n.1090C=
NR_047695.2:n.861C=