Canonical Allele Identifier: CA2333177828

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399780G= , CM000681.2:g.34399780G=	GRCh38
NC_000019.9:g.34890685G= , CM000681.1:g.34890685G=	GRCh37
NC_000019.8:g.39582525G=	NCBI36
NG_012838.2:g.40041G=
NG_012838.3:g.45189G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1536G= MANE Select	ENSP00000348877.3:p.Gln512=
ENST00000415930.8:c.1653G=	ENSP00000405573.3:p.Gln551=
ENST00000586425.2:c.1202G=
ENST00000588991.7:c.1569G=	ENSP00000465858.3:p.Gln523=
ENST00000643067.1:n.2581G=
ENST00000647446.1:c.*587G=	ENSP00000495129.1:n.*587G=
ENST00000356487.9:c.1536G=	ENSP00000348877.3:p.Gln512=
ENST00000415930.7:c.1569G=	ENSP00000405573.2:p.Gln523=
ENST00000586077.1:n.2498G=
ENST00000586392.1:n.1274G=
ENST00000586425.1:c.1399-121G=	ENSP00000467670.2:n.1399-121G=
ENST00000588991.6:c.1581G=	ENSP00000465858.2:p.Gln527=
ENST00000592740.5:c.193+3123G=
NM_000175.3:c.1536G=	NP_000166.2:p.Gln512=
NM_001184722.1:c.1569G=	NP_001171651.1:p.Gln523=
NM_001289789.1:c.1653G=	NP_001276718.1:p.Gln551=
NM_001289790.1:c.1452G=	NP_001276719.1:p.Gln484=
XM_005258764.1:c.1536G=	XP_005258821.1:p.Gln512=
XM_006723148.1:c.1536G=	XP_006723211.1:p.Gln512=
XM_011526754.1:c.1653G=	XP_011525056.1:p.Gln551=
NM_000175.5:c.1536G= MANE Select	NP_000166.2:p.Gln512=
NM_001289790.2:c.1452G=	NP_001276719.1:p.Gln484=
NM_001329909.1:c.1536G=	NP_001316838.1:p.Gln512=
NM_001329910.1:c.1536G=	NP_001316839.1:p.Gln512=
NM_001329911.1:c.1509G=	NP_001316840.1:p.Gln503=
XM_011526754.3:c.1653G=	XP_011525056.1:p.Gln551=
NM_001289790.3:c.1452G=	NP_001276719.1:p.Gln484=
NM_001329911.2:c.1509G=	NP_001316840.1:p.Gln503=