Canonical Allele Identifier: CA2333177908

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399969C= , CM000681.2:g.34399969C=	GRCh38
NC_000019.9:g.34890874C= , CM000681.1:g.34890874C=	GRCh37
NC_000019.8:g.39582714C=	NCBI36
NG_012838.2:g.40230C=
NG_012838.3:g.45378C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1610C= MANE Select	ENSP00000348877.3:p.Ser537=
ENST00000415930.8:c.1727C=	ENSP00000405573.3:p.Ser576=
ENST00000586425.2:c.1276C=
ENST00000588991.7:c.1643C=	ENSP00000465858.3:p.Ser548=
ENST00000643067.1:n.2655C=
ENST00000647446.1:c.*661C=	ENSP00000495129.1:n.*661C=
ENST00000356487.9:c.1610C=	ENSP00000348877.3:p.Ser537=
ENST00000415930.7:c.1643C=	ENSP00000405573.2:p.Ser548=
ENST00000586077.1:n.2687C=
ENST00000586392.1:n.1348C=
ENST00000586425.1:c.*42C=	ENSP00000467670.2:n.*42C=
ENST00000588991.6:c.1655C=	ENSP00000465858.2:p.Ser552=
ENST00000592740.5:c.193+3312C=
NM_000175.3:c.1610C=	NP_000166.2:p.Ser537=
NM_001184722.1:c.1643C=	NP_001171651.1:p.Ser548=
NM_001289789.1:c.1727C=	NP_001276718.1:p.Ser576=
NM_001289790.1:c.1526C=	NP_001276719.1:p.Ser509=
XM_005258764.1:c.1610C=	XP_005258821.1:p.Ser537=
XM_006723148.1:c.1610C=	XP_006723211.1:p.Ser537=
XM_011526754.1:c.1727C=	XP_011525056.1:p.Ser576=
NM_000175.5:c.1610C= MANE Select	NP_000166.2:p.Ser537=
NM_001289790.2:c.1526C=	NP_001276719.1:p.Ser509=
NM_001329909.1:c.1610C=	NP_001316838.1:p.Ser537=
NM_001329910.1:c.1610C=	NP_001316839.1:p.Ser537=
NM_001329911.1:c.1583C=	NP_001316840.1:p.Ser528=
XM_011526754.3:c.1727C=	XP_011525056.1:p.Ser576=
NM_001289790.3:c.1526C=	NP_001276719.1:p.Ser509=
NM_001329911.2:c.1583C=	NP_001316840.1:p.Ser528=