Canonical Allele Identifier: CA2333177913
Gene: GPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.34399976C= , CM000681.2:g.34399976C= GRCh38
NC_000019.9:g.34890881C= , CM000681.1:g.34890881C= GRCh37
NC_000019.8:g.39582721C= NCBI36
NG_012838.2:g.40237C=
NG_012838.3:g.45385C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356487.11:c.1617C= MANE Select ENSP00000348877.3:p.Asp539=
ENST00000415930.8:c.1734C= ENSP00000405573.3:p.Asp578=
ENST00000586425.2:c.1283C=
ENST00000588991.7:c.1650C= ENSP00000465858.3:p.Asp550=
ENST00000643067.1:n.2662C=
ENST00000647446.1:c.*668C= ENSP00000495129.1:n.*668C=
ENST00000356487.9:c.1617C= ENSP00000348877.3:p.Asp539=
ENST00000415930.7:c.1650C= ENSP00000405573.2:p.Asp550=
ENST00000586077.1:n.2694C=
ENST00000586392.1:n.1355C=
ENST00000586425.1:c.*49C= ENSP00000467670.2:n.*49C=
ENST00000588991.6:c.1662C= ENSP00000465858.2:p.Asp554=
ENST00000592740.5:c.193+3319C=
NM_000175.3:c.1617C= NP_000166.2:p.Asp539=
NM_001184722.1:c.1650C= NP_001171651.1:p.Asp550=
NM_001289789.1:c.1734C= NP_001276718.1:p.Asp578=
NM_001289790.1:c.1533C= NP_001276719.1:p.Asp511=
XM_005258764.1:c.1617C= XP_005258821.1:p.Asp539=
XM_006723148.1:c.1617C= XP_006723211.1:p.Asp539=
XM_011526754.1:c.1734C= XP_011525056.1:p.Asp578=
NM_000175.5:c.1617C= MANE Select NP_000166.2:p.Asp539=
NM_001289790.2:c.1533C= NP_001276719.1:p.Asp511=
NM_001329909.1:c.1617C= NP_001316838.1:p.Asp539=
NM_001329910.1:c.1617C= NP_001316839.1:p.Asp539=
NM_001329911.1:c.1590C= NP_001316840.1:p.Asp530=
XM_011526754.3:c.1734C= XP_011525056.1:p.Asp578=
NM_001289790.3:c.1533C= NP_001276719.1:p.Asp511=
NM_001329911.2:c.1590C= NP_001316840.1:p.Asp530=