Canonical Allele Identifier: CA2333177942

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400029T= , CM000681.2:g.34400029T=	GRCh38
NC_000019.9:g.34890934T= , CM000681.1:g.34890934T=	GRCh37
NC_000019.8:g.39582774T=	NCBI36
NG_012838.2:g.40290T=
NG_012838.3:g.45438T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1670T= MANE Select	ENSP00000348877.3:p.Val557=
ENST00000415930.8:c.1787T=	ENSP00000405573.3:p.Val596=
ENST00000586425.2:c.1336T=
ENST00000588991.7:c.1703T=	ENSP00000465858.3:p.Val568=
ENST00000643067.1:n.2715T=
ENST00000647446.1:c.*721T=	ENSP00000495129.1:n.*721T=
ENST00000356487.9:c.1670T=	ENSP00000348877.3:p.Val557=
ENST00000415930.7:c.1703T=	ENSP00000405573.2:p.Val568=
ENST00000586077.1:n.2747T=
ENST00000586392.1:n.1408T=
ENST00000586425.1:c.*102T=	ENSP00000467670.2:n.*102T=
ENST00000588991.6:c.1715T=	ENSP00000465858.2:p.Val572=
ENST00000592740.5:c.193+3372T=
NM_000175.3:c.1670T=	NP_000166.2:p.Val557=
NM_001184722.1:c.1703T=	NP_001171651.1:p.Val568=
NM_001289789.1:c.1787T=	NP_001276718.1:p.Val596=
NM_001289790.1:c.1586T=	NP_001276719.1:p.Val529=
XM_005258764.1:c.1670T=	XP_005258821.1:p.Val557=
XM_006723148.1:c.1670T=	XP_006723211.1:p.Val557=
XM_011526754.1:c.1787T=	XP_011525056.1:p.Val596=
NM_000175.5:c.1670T= MANE Select	NP_000166.2:p.Val557=
NM_001289790.2:c.1586T=	NP_001276719.1:p.Val529=
NM_001329909.1:c.1670T=	NP_001316838.1:p.Val557=
NM_001329910.1:c.1670T=	NP_001316839.1:p.Val557=
NM_001329911.1:c.1643T=	NP_001316840.1:p.Val548=
XM_011526754.3:c.1787T=	XP_011525056.1:p.Val596=
NM_001289790.3:c.1586T=	NP_001276719.1:p.Val529=
NM_001329911.2:c.1643T=	NP_001316840.1:p.Val548=