Canonical Allele Identifier: CA409170182
Gene: PIGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45424239C>A , CM000682.2:g.45424239C>A GRCh38
NC_000020.10:g.44052879C>A , CM000682.1:g.44052879C>A GRCh37
NC_000020.9:g.43486293C>A NCBI36
NG_047154.1:g.13173C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000424705.3:c.1258C>A ENSP00000491856.2:p.Gln420Lys
ENST00000638691.2:c.1258C>A ENSP00000492094.2:p.Gln420Lys
ENST00000639292.2:c.1339C>A ENSP00000491678.2:p.Gln447Lys
ENST00000640549.2:c.1258C>A ENSP00000492043.2:p.Gln420Lys
ENST00000687237.1:n.648C>A
ENST00000689203.1:c.1258C>A ENSP00000508682.1:p.Gln420Lys
ENST00000690879.1:n.734C>A
ENST00000692236.1:c.1258C>A ENSP00000509421.1:p.Gln420Lys
ENST00000279035.14:c.952C>A ENSP00000279035.8:p.Gln318Lys
ENST00000279036.12:c.1258C>A MANE Select ENSP00000279036.6:p.Gln420Lys
ENST00000432270.2:c.751C>A ENSP00000408354.2:p.Gln251Lys
ENST00000543458.7:c.1090C>A ENSP00000441577.1:p.Gln364Lys
ENST00000545755.3:c.676C>A ENSP00000443963.3:p.Gln226Lys
ENST00000638241.1:n.1136C>A
ENST00000638246.1:c.*758C>A ENSP00000492883.1:n.*758C>A
ENST00000638277.1:c.192C>A
ENST00000638383.1:c.*607C>A ENSP00000492295.1:n.*607C>A
ENST00000638387.1:c.*302C>A ENSP00000492873.1:n.*302C>A
ENST00000638415.1:c.795C>A
ENST00000638445.1:c.*642C>A ENSP00000491297.1:n.*642C>A
ENST00000638537.1:n.1047C>A
ENST00000638594.1:c.1258C>A ENSP00000491697.1:p.Gln420Lys
ENST00000638612.1:c.1258C>A ENSP00000491458.1:p.Gln420Lys
ENST00000638671.1:c.*642C>A ENSP00000492875.1:n.*642C>A
ENST00000638689.1:n.3465C>A
ENST00000638691.1:c.15C>A
ENST00000638710.1:c.1464C>A ENSP00000491406.1:n.1464C>A
ENST00000638714.1:c.*642C>A ENSP00000491194.1:n.*642C>A
ENST00000638745.1:c.*642C>A ENSP00000491744.1:n.*642C>A
ENST00000638927.1:c.400C>A ENSP00000492335.1:p.Gln134Lys
ENST00000638938.1:c.*714C>A ENSP00000491171.1:n.*714C>A
ENST00000638962.1:n.1218C>A
ENST00000638978.1:c.1208C>A ENSP00000492743.1:p.Pro403Gln
ENST00000639250.1:n.2508C>A
ENST00000639292.1:c.1118C>A
ENST00000639382.1:c.1117C>A ENSP00000491534.1:p.Gln373Lys
ENST00000639417.1:c.*302C>A ENSP00000491058.1:n.*302C>A
ENST00000639499.1:c.1258C>A ENSP00000491170.1:p.Gln420Lys
ENST00000639664.1:n.985C>A
ENST00000639783.1:c.*560C>A ENSP00000491772.1:n.*560C>A
ENST00000639872.1:n.827C>A
ENST00000639932.1:c.*560C>A ENSP00000491600.1:n.*560C>A
ENST00000639984.1:c.*560C>A ENSP00000492727.1:n.*560C>A
ENST00000640107.1:c.*518C>A ENSP00000491118.1:n.*518C>A
ENST00000640108.1:c.*947C>A ENSP00000492007.1:n.*947C>A
ENST00000640175.1:c.*560C>A ENSP00000492418.1:n.*560C>A
ENST00000640194.1:c.*577C>A ENSP00000492279.1:n.*577C>A
ENST00000640210.1:c.847C>A ENSP00000491164.1:p.Gln283Lys
ENST00000640253.1:n.472C>A
ENST00000640272.1:c.*642C>A ENSP00000492270.1:n.*642C>A
ENST00000640324.1:c.1264C>A ENSP00000491074.1:p.Gln422Lys
ENST00000640364.1:n.1981C>A
ENST00000640542.1:c.1057C>A ENSP00000492174.1:p.Gln353Lys
ENST00000640549.1:c.748C>A ENSP00000492043.1:p.Gln250Lys
ENST00000640585.1:c.*915C>A ENSP00000491308.1:n.*915C>A
ENST00000640638.1:n.426C>A
ENST00000640666.1:c.1258C>A ENSP00000491072.1:p.Gln420Lys
ENST00000640692.1:c.*174C>A ENSP00000492370.1:n.*174C>A
ENST00000640940.1:n.920C>A
ENST00000640986.1:c.*375C>A ENSP00000491886.1:n.*375C>A
ENST00000640996.1:c.*935C>A ENSP00000492464.1:n.*935C>A
ENST00000279035.13:c.952C>A ENSP00000279035.8:p.Gln318Lys
ENST00000279036.10:c.1258C>A ENSP00000279036.6:p.Gln420Lys
ENST00000372689.9:c.1057C>A ENSP00000361774.4:p.Gln353Lys
ENST00000455050.2:c.*789C>A ENSP00000407574.2:n.*789C>A
ENST00000543458.6:c.1090C>A ENSP00000441577.1:p.Gln364Lys
ENST00000545755.2:c.287C>A
NM_001184728.2:c.1090C>A NP_001171657.1:p.Gln364Lys
NM_001184729.2:c.1057C>A NP_001171658.1:p.Gln353Lys
NM_001184730.2:c.952C>A NP_001171659.1:p.Gln318Lys
NM_015937.5:c.1258C>A NP_057021.2:p.Gln420Lys
NR_047691.1:n.1308C>A
NR_047692.1:n.1251C>A
NR_047693.1:n.1247C>A
NR_047694.1:n.1170C>A
NR_047695.1:n.941C>A
XM_005260430.2:c.751C>A XP_005260487.1:p.Gln251Lys
XM_005260432.1:c.472C>A XP_005260489.1:p.Gln158Lys
XM_005260432.3:c.472C>A XP_005260489.1:p.Gln158Lys
XR_001754286.2:n.1294C>A
XR_001754287.2:n.1093C>A
NM_015937.6:c.1258C>A MANE Select NP_057021.2:p.Gln420Lys
NM_001184728.3:c.1090C>A NP_001171657.1:p.Gln364Lys
NM_001184729.3:c.1057C>A NP_001171658.1:p.Gln353Lys
NM_001184730.3:c.952C>A NP_001171659.1:p.Gln318Lys
NR_047691.2:n.1234C>A
NR_047692.2:n.1177C>A
NR_047693.2:n.1173C>A
NR_047694.2:n.1096C>A
NR_047695.2:n.867C>A