Canonical Allele Identifier: CA2333177917
Gene: GPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.34399984C= , CM000681.2:g.34399984C= GRCh38
NC_000019.9:g.34890889C= , CM000681.1:g.34890889C= GRCh37
NC_000019.8:g.39582729C= NCBI36
NG_012838.2:g.40245C=
NG_012838.3:g.45393C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356487.11:c.1625C= MANE Select ENSP00000348877.3:p.Thr542=
ENST00000415930.8:c.1742C= ENSP00000405573.3:p.Thr581=
ENST00000586425.2:c.1291C=
ENST00000588991.7:c.1658C= ENSP00000465858.3:p.Thr553=
ENST00000643067.1:n.2670C=
ENST00000647446.1:c.*676C= ENSP00000495129.1:n.*676C=
ENST00000356487.9:c.1625C= ENSP00000348877.3:p.Thr542=
ENST00000415930.7:c.1658C= ENSP00000405573.2:p.Thr553=
ENST00000586077.1:n.2702C=
ENST00000586392.1:n.1363C=
ENST00000586425.1:c.*57C= ENSP00000467670.2:n.*57C=
ENST00000588991.6:c.1670C= ENSP00000465858.2:p.Thr557=
ENST00000592740.5:c.193+3327C=
NM_000175.3:c.1625C= NP_000166.2:p.Thr542=
NM_001184722.1:c.1658C= NP_001171651.1:p.Thr553=
NM_001289789.1:c.1742C= NP_001276718.1:p.Thr581=
NM_001289790.1:c.1541C= NP_001276719.1:p.Thr514=
XM_005258764.1:c.1625C= XP_005258821.1:p.Thr542=
XM_006723148.1:c.1625C= XP_006723211.1:p.Thr542=
XM_011526754.1:c.1742C= XP_011525056.1:p.Thr581=
NM_000175.5:c.1625C= MANE Select NP_000166.2:p.Thr542=
NM_001289790.2:c.1541C= NP_001276719.1:p.Thr514=
NM_001329909.1:c.1625C= NP_001316838.1:p.Thr542=
NM_001329910.1:c.1625C= NP_001316839.1:p.Thr542=
NM_001329911.1:c.1598C= NP_001316840.1:p.Thr533=
XM_011526754.3:c.1742C= XP_011525056.1:p.Thr581=
NM_001289790.3:c.1541C= NP_001276719.1:p.Thr514=
NM_001329911.2:c.1598C= NP_001316840.1:p.Thr533=