Canonical Allele Identifier: CA2333177896

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399943G= , CM000681.2:g.34399943G=	GRCh38
NC_000019.9:g.34890848G= , CM000681.1:g.34890848G=	GRCh37
NC_000019.8:g.39582688G=	NCBI36
NG_012838.2:g.40204G=
NG_012838.3:g.45352G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1584G= MANE Select	ENSP00000348877.3:p.Glu528=
ENST00000415930.8:c.1701G=	ENSP00000405573.3:p.Glu567=
ENST00000586425.2:c.1250G=
ENST00000588991.7:c.1617G=	ENSP00000465858.3:p.Glu539=
ENST00000643067.1:n.2629G=
ENST00000647446.1:c.*635G=	ENSP00000495129.1:n.*635G=
ENST00000356487.9:c.1584G=	ENSP00000348877.3:p.Glu528=
ENST00000415930.7:c.1617G=	ENSP00000405573.2:p.Glu539=
ENST00000586077.1:n.2661G=
ENST00000586392.1:n.1322G=
ENST00000586425.1:c.*16G=	ENSP00000467670.2:n.*16G=
ENST00000588991.6:c.1629G=	ENSP00000465858.2:p.Glu543=
ENST00000592740.5:c.193+3286G=
NM_000175.3:c.1584G=	NP_000166.2:p.Glu528=
NM_001184722.1:c.1617G=	NP_001171651.1:p.Glu539=
NM_001289789.1:c.1701G=	NP_001276718.1:p.Glu567=
NM_001289790.1:c.1500G=	NP_001276719.1:p.Glu500=
XM_005258764.1:c.1584G=	XP_005258821.1:p.Glu528=
XM_006723148.1:c.1584G=	XP_006723211.1:p.Glu528=
XM_011526754.1:c.1701G=	XP_011525056.1:p.Glu567=
NM_000175.5:c.1584G= MANE Select	NP_000166.2:p.Glu528=
NM_001289790.2:c.1500G=	NP_001276719.1:p.Glu500=
NM_001329909.1:c.1584G=	NP_001316838.1:p.Glu528=
NM_001329910.1:c.1584G=	NP_001316839.1:p.Glu528=
NM_001329911.1:c.1557G=	NP_001316840.1:p.Glu519=
XM_011526754.3:c.1701G=	XP_011525056.1:p.Glu567=
NM_001289790.3:c.1500G=	NP_001276719.1:p.Glu500=
NM_001329911.2:c.1557G=	NP_001316840.1:p.Glu519=