Canonical Allele Identifier: CA2333177746

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399569A= , CM000681.2:g.34399569A=	GRCh38
NC_000019.9:g.34890474A= , CM000681.1:g.34890474A=	GRCh37
NC_000019.8:g.39582314A=	NCBI36
NG_012838.2:g.39830A=
NG_012838.3:g.44978A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1412A= MANE Select	ENSP00000348877.3:p.Asn471=
ENST00000415930.8:c.1529A=	ENSP00000405573.3:p.Asn510=
ENST00000586425.2:c.1158-167A=
ENST00000588991.7:c.1445A=	ENSP00000465858.3:p.Asn482=
ENST00000643067.1:n.2457A=
ENST00000647446.1:c.*463A=	ENSP00000495129.1:n.*463A=
ENST00000356487.9:c.1412A=	ENSP00000348877.3:p.Asn471=
ENST00000415930.7:c.1445A=	ENSP00000405573.2:p.Asn482=
ENST00000586077.1:n.2287A=
ENST00000586392.1:n.1150A=
ENST00000586425.1:c.1398+234A=	ENSP00000467670.2:n.1398+234A=
ENST00000588991.6:c.1457A=	ENSP00000465858.2:p.Asn486=
ENST00000592740.5:c.193+2912A=
NM_000175.3:c.1412A=	NP_000166.2:p.Asn471=
NM_001184722.1:c.1445A=	NP_001171651.1:p.Asn482=
NM_001289789.1:c.1529A=	NP_001276718.1:p.Asn510=
NM_001289790.1:c.1328A=	NP_001276719.1:p.Asn443=
XM_005258764.1:c.1412A=	XP_005258821.1:p.Asn471=
XM_006723148.1:c.1412A=	XP_006723211.1:p.Asn471=
XM_011526754.1:c.1529A=	XP_011525056.1:p.Asn510=
NM_000175.5:c.1412A= MANE Select	NP_000166.2:p.Asn471=
NM_001289790.2:c.1328A=	NP_001276719.1:p.Asn443=
NM_001329909.1:c.1412A=	NP_001316838.1:p.Asn471=
NM_001329910.1:c.1412A=	NP_001316839.1:p.Asn471=
NM_001329911.1:c.1385A=	NP_001316840.1:p.Asn462=
XM_011526754.3:c.1529A=	XP_011525056.1:p.Asn510=
NM_001289790.3:c.1328A=	NP_001276719.1:p.Asn443=
NM_001329911.2:c.1385A=	NP_001316840.1:p.Asn462=