Canonical Allele Identifier: CA2333177964

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400083C= , CM000681.2:g.34400083C=	GRCh38
NC_000019.9:g.34890988C= , CM000681.1:g.34890988C=	GRCh37
NC_000019.8:g.39582828C=	NCBI36
NG_012838.2:g.40344C=
NG_012838.3:g.45492C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.*47C= MANE Select	ENSP00000348877.3:n.*47C=
ENST00000415930.8:c.*47C=	ENSP00000405573.3:n.*47C=
ENST00000586425.2:c.1390C=
ENST00000588991.7:c.*47C=	ENSP00000465858.3:n.*47C=
ENST00000643067.1:n.2769C=
ENST00000647446.1:c.*775C=	ENSP00000495129.1:n.*775C=
ENST00000356487.9:c.*47C=	ENSP00000348877.3:n.*47C=
ENST00000415930.7:c.*47C=	ENSP00000405573.2:n.*47C=
ENST00000586077.1:n.2801C=
ENST00000586392.1:n.1462C=
ENST00000586425.1:c.*156C=	ENSP00000467670.2:n.*156C=
ENST00000588991.6:c.1769C=	ENSP00000465858.2:n.1769C=
ENST00000592740.5:c.193+3426C=
NM_000175.3:c.*47C=	NP_000166.2:n.*47C=
NM_001184722.1:c.*47C=	NP_001171651.1:n.*47C=
NM_001289789.1:c.*47C=	NP_001276718.1:n.*47C=
NM_001289790.1:c.*47C=	NP_001276719.1:n.*47C=
XM_005258764.1:c.*47C=	XP_005258821.1:n.*47C=
XM_006723148.1:c.*47C=	XP_006723211.1:n.*47C=
XM_011526754.1:c.*47C=	XP_011525056.1:n.*47C=
NM_000175.5:c.*47C= MANE Select	NP_000166.2:n.*47C=
NM_001289790.2:c.*47C=	NP_001276719.1:n.*47C=
NM_001329909.1:c.*47C=	NP_001316838.1:n.*47C=
NM_001329910.1:c.*47C=	NP_001316839.1:n.*47C=
NM_001329911.1:c.*47C=	NP_001316840.1:n.*47C=
XM_011526754.3:c.*47C=	XP_011525056.1:n.*47C=
NM_001289790.3:c.*47C=	NP_001276719.1:n.*47C=
NM_001329911.2:c.*47C=	NP_001316840.1:n.*47C=