Canonical Allele Identifier: CA2333177922

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399992C= , CM000681.2:g.34399992C=	GRCh38
NC_000019.9:g.34890897C= , CM000681.1:g.34890897C=	GRCh37
NC_000019.8:g.39582737C=	NCBI36
NG_012838.2:g.40253C=
NG_012838.3:g.45401C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1633C= MANE Select	ENSP00000348877.3:p.Leu545=
ENST00000415930.8:c.1750C=	ENSP00000405573.3:p.Leu584=
ENST00000586425.2:c.1299C=
ENST00000588991.7:c.1666C=	ENSP00000465858.3:p.Leu556=
ENST00000643067.1:n.2678C=
ENST00000647446.1:c.*684C=	ENSP00000495129.1:n.*684C=
ENST00000356487.9:c.1633C=	ENSP00000348877.3:p.Leu545=
ENST00000415930.7:c.1666C=	ENSP00000405573.2:p.Leu556=
ENST00000586077.1:n.2710C=
ENST00000586392.1:n.1371C=
ENST00000586425.1:c.*65C=	ENSP00000467670.2:n.*65C=
ENST00000588991.6:c.1678C=	ENSP00000465858.2:p.Leu560=
ENST00000592740.5:c.193+3335C=
NM_000175.3:c.1633C=	NP_000166.2:p.Leu545=
NM_001184722.1:c.1666C=	NP_001171651.1:p.Leu556=
NM_001289789.1:c.1750C=	NP_001276718.1:p.Leu584=
NM_001289790.1:c.1549C=	NP_001276719.1:p.Leu517=
XM_005258764.1:c.1633C=	XP_005258821.1:p.Leu545=
XM_006723148.1:c.1633C=	XP_006723211.1:p.Leu545=
XM_011526754.1:c.1750C=	XP_011525056.1:p.Leu584=
NM_000175.5:c.1633C= MANE Select	NP_000166.2:p.Leu545=
NM_001289790.2:c.1549C=	NP_001276719.1:p.Leu517=
NM_001329909.1:c.1633C=	NP_001316838.1:p.Leu545=
NM_001329910.1:c.1633C=	NP_001316839.1:p.Leu545=
NM_001329911.1:c.1606C=	NP_001316840.1:p.Leu536=
XM_011526754.3:c.1750C=	XP_011525056.1:p.Leu584=
NM_001289790.3:c.1549C=	NP_001276719.1:p.Leu517=
NM_001329911.2:c.1606C=	NP_001316840.1:p.Leu536=