Canonical Allele Identifier: CA2333167688

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34378981G= , CM000681.2:g.34378981G=	GRCh38
NC_000019.9:g.34869886G= , CM000681.1:g.34869886G=	GRCh37
NC_000019.8:g.39561726G=	NCBI36
NG_012838.2:g.19242G=
NG_012838.3:g.24390G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.681G= MANE Select	ENSP00000348877.3:p.Glu227=
ENST00000415930.8:c.798G=	ENSP00000405573.3:p.Glu266=
ENST00000586425.2:c.569G=
ENST00000588991.7:c.714G=	ENSP00000465858.3:p.Glu238=
ENST00000589399.6:c.450G=	ENSP00000468201.2:p.Glu150=
ENST00000643067.1:n.1191G=
ENST00000647446.1:c.681G=	ENSP00000495129.1:p.Glu227=
ENST00000356487.9:c.681G=	ENSP00000348877.3:p.Glu227=
ENST00000415930.7:c.714G=	ENSP00000405573.2:p.Glu238=
ENST00000586425.1:c.681G=	ENSP00000467670.2:p.Glu227=
ENST00000588991.6:c.726G=	ENSP00000465858.2:p.Glu242=
ENST00000590362.1:n.4G=
NM_000175.3:c.681G=	NP_000166.2:p.Glu227=
NM_001184722.1:c.714G=	NP_001171651.1:p.Glu238=
NM_001289789.1:c.798G=	NP_001276718.1:p.Glu266=
NM_001289790.1:c.597G=	NP_001276719.1:p.Glu199=
XM_005258764.1:c.681G=	XP_005258821.1:p.Glu227=
XM_006723148.1:c.681G=	XP_006723211.1:p.Glu227=
XM_011526754.1:c.798G=	XP_011525056.1:p.Glu266=
XM_011526755.1:c.798G=	XP_011525057.1:p.Glu266=
NM_000175.5:c.681G= MANE Select	NP_000166.2:p.Glu227=
NM_001289790.2:c.597G=	NP_001276719.1:p.Glu199=
NM_001329909.1:c.681G=	NP_001316838.1:p.Glu227=
NM_001329910.1:c.681G=	NP_001316839.1:p.Glu227=
NM_001329911.1:c.681G=	NP_001316840.1:p.Glu227=
XM_011526754.3:c.798G=	XP_011525056.1:p.Glu266=
NM_001289790.3:c.597G=	NP_001276719.1:p.Glu199=
NM_001329911.2:c.681G=	NP_001316840.1:p.Glu227=