Canonical Allele Identifier: CA9877914
Gene: PIGT HGNC NCBI

Linked Data

ClinVar Variation Id: 541407
dbSNP Id: rs201944222

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45419290C>T , CM000682.2:g.45419290C>T GRCh38
NC_000020.10:g.44047930C>T , CM000682.1:g.44047930C>T GRCh37
NC_000020.9:g.43481344C>T NCBI36
NG_047154.1:g.8224C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000424705.3:c.494-5C>T ENSP00000491856.2:n.494-5C>T
ENST00000638691.2:c.494-5C>T ENSP00000492094.2:n.494-5C>T
ENST00000639292.2:c.494-5C>T ENSP00000491678.2:n.494-5C>T
ENST00000640549.2:c.494-5C>T ENSP00000492043.2:n.494-5C>T
ENST00000689203.1:c.494-5C>T ENSP00000508682.1:n.494-5C>T
ENST00000692236.1:c.494-5C>T ENSP00000509421.1:n.494-5C>T
ENST00000279035.14:c.188-5C>T ENSP00000279035.8:n.188-5C>T
ENST00000279036.12:c.494-5C>T MANE Select ENSP00000279036.6:n.494-5C>T
ENST00000432270.2:c.188-5C>T ENSP00000408354.2:n.188-5C>T
ENST00000543458.7:c.326-5C>T ENSP00000441577.1:n.326-5C>T
ENST00000545755.3:c.188-1042C>T ENSP00000443963.3:n.188-1042C>T
ENST00000638246.1:c.366-5C>T ENSP00000492883.1:n.366-5C>T
ENST00000638353.1:c.316-214C>T ENSP00000491538.1:n.316-214C>T
ENST00000638383.1:c.494-5C>T ENSP00000492295.1:n.494-5C>T
ENST00000638387.1:c.494-5C>T ENSP00000492873.1:n.494-5C>T
ENST00000638415.1:c.31-5C>T
ENST00000638445.1:c.454-5C>T ENSP00000491297.1:n.454-5C>T
ENST00000638478.1:c.494-218C>T ENSP00000491233.1:n.494-218C>T
ENST00000638489.1:c.464-5C>T ENSP00000491566.1:n.464-5C>T
ENST00000638537.1:n.283-5C>T
ENST00000638594.1:c.494-5C>T ENSP00000491697.1:n.494-5C>T
ENST00000638612.1:c.494-5C>T ENSP00000491458.1:n.494-5C>T
ENST00000638671.1:c.316-5C>T ENSP00000492875.1:n.316-5C>T
ENST00000638689.1:n.2681-5C>T
ENST00000638710.1:c.695C>T ENSP00000491406.1:n.695C>T
ENST00000638714.1:c.366-214C>T ENSP00000491194.1:n.366-214C>T
ENST00000638745.1:c.316-5C>T ENSP00000491744.1:n.316-5C>T
ENST00000638938.1:c.*151-5C>T ENSP00000491171.1:n.*151-5C>T
ENST00000638953.1:c.*151-5C>T ENSP00000492848.1:n.*151-5C>T
ENST00000638962.1:n.454-5C>T
ENST00000638978.1:c.494-5C>T ENSP00000492743.1:n.494-5C>T
ENST00000639194.1:c.240-5C>T ENSP00000492210.1:n.240-5C>T
ENST00000639235.1:c.378C>T ENSP00000492498.1:p.Pro126=
ENST00000639250.1:n.1050C>T
ENST00000639286.1:c.188-5C>T ENSP00000492507.1:n.188-5C>T
ENST00000639292.1:c.273-5C>T
ENST00000639382.1:c.454-214C>T ENSP00000491534.1:n.454-214C>T
ENST00000639417.1:c.366-1042C>T ENSP00000491058.1:n.366-1042C>T
ENST00000639499.1:c.494-5C>T ENSP00000491170.1:n.494-5C>T
ENST00000639664.1:n.221-5C>T
ENST00000639783.1:c.494-214C>T ENSP00000491772.1:n.494-214C>T
ENST00000639932.1:c.494-5C>T ENSP00000491600.1:n.494-5C>T
ENST00000639984.1:c.316-5C>T ENSP00000492727.1:n.316-5C>T
ENST00000640107.1:c.494-5C>T ENSP00000491118.1:n.494-5C>T
ENST00000640108.1:c.*183-5C>T ENSP00000492007.1:n.*183-5C>T
ENST00000640175.1:c.188-214C>T ENSP00000492418.1:n.188-214C>T
ENST00000640194.1:c.366-5C>T ENSP00000492279.1:n.366-5C>T
ENST00000640210.1:c.188-218C>T ENSP00000491164.1:n.188-218C>T
ENST00000640272.1:c.494-5C>T ENSP00000492270.1:n.494-5C>T
ENST00000640324.1:c.495C>T ENSP00000491074.1:p.Pro165=
ENST00000640364.1:n.528-5C>T
ENST00000640542.1:c.494-5C>T ENSP00000492174.1:n.494-5C>T
ENST00000640585.1:c.*151-5C>T ENSP00000491308.1:n.*151-5C>T
ENST00000640666.1:c.494-5C>T ENSP00000491072.1:n.494-5C>T
ENST00000640692.1:c.494-5C>T ENSP00000492370.1:n.494-5C>T
ENST00000640940.1:n.156-5C>T
ENST00000640986.1:c.494-5C>T ENSP00000491886.1:n.494-5C>T
ENST00000640996.1:c.*151-5C>T ENSP00000492464.1:n.*151-5C>T
ENST00000279035.13:c.188-5C>T ENSP00000279035.8:n.188-5C>T
ENST00000279036.10:c.494-5C>T ENSP00000279036.6:n.494-5C>T
ENST00000372689.9:c.494-5C>T ENSP00000361774.4:n.494-5C>T
ENST00000432270.1:c.162-1042C>T
ENST00000455050.2:c.366-5C>T ENSP00000407574.2:n.366-5C>T
ENST00000543458.6:c.326-5C>T ENSP00000441577.1:n.326-5C>T
NM_001184728.2:c.326-5C>T NP_001171657.1:n.326-5C>T
NM_001184729.2:c.494-5C>T NP_001171658.1:n.494-5C>T
NM_001184730.2:c.188-5C>T NP_001171659.1:n.188-5C>T
NM_015937.5:c.494-5C>T NP_057021.2:n.494-5C>T
NR_047691.1:n.544-5C>T
NR_047692.1:n.456-5C>T
NR_047693.1:n.584-214C>T
NR_047694.1:n.406-5C>T
NR_047695.1:n.278-214C>T
XM_005260430.2:c.188-5C>T XP_005260487.1:n.188-5C>T
XM_005260432.1:c.-293-5C>T XP_005260489.1:n.-293-5C>T
XM_005260432.3:c.-293-5C>T XP_005260489.1:n.-293-5C>T
XR_001754286.2:n.510-5C>T
XR_001754287.2:n.510-5C>T
NM_015937.6:c.494-5C>T MANE Select NP_057021.2:n.494-5C>T
NM_001184728.3:c.326-5C>T NP_001171657.1:n.326-5C>T
NM_001184729.3:c.494-5C>T NP_001171658.1:n.494-5C>T
NM_001184730.3:c.188-5C>T NP_001171659.1:n.188-5C>T
NR_047691.2:n.470-5C>T
NR_047692.2:n.382-5C>T
NR_047693.2:n.510-214C>T
NR_047694.2:n.332-5C>T
NR_047695.2:n.204-214C>T