Canonical Allele Identifier: CA2333177956

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400067C= , CM000681.2:g.34400067C=	GRCh38
NC_000019.9:g.34890972C= , CM000681.1:g.34890972C=	GRCh37
NC_000019.8:g.39582812C=	NCBI36
NG_012838.2:g.40328C=
NG_012838.3:g.45476C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.*31C= MANE Select	ENSP00000348877.3:n.*31C=
ENST00000415930.8:c.*31C=	ENSP00000405573.3:n.*31C=
ENST00000586425.2:c.1374C=
ENST00000588991.7:c.*31C=	ENSP00000465858.3:n.*31C=
ENST00000643067.1:n.2753C=
ENST00000647446.1:c.*759C=	ENSP00000495129.1:n.*759C=
ENST00000356487.9:c.*31C=	ENSP00000348877.3:n.*31C=
ENST00000415930.7:c.*31C=	ENSP00000405573.2:n.*31C=
ENST00000586077.1:n.2785C=
ENST00000586392.1:n.1446C=
ENST00000586425.1:c.*140C=	ENSP00000467670.2:n.*140C=
ENST00000588991.6:c.1753C=	ENSP00000465858.2:n.1753C=
ENST00000592740.5:c.193+3410C=
NM_000175.3:c.*31C=	NP_000166.2:n.*31C=
NM_001184722.1:c.*31C=	NP_001171651.1:n.*31C=
NM_001289789.1:c.*31C=	NP_001276718.1:n.*31C=
NM_001289790.1:c.*31C=	NP_001276719.1:n.*31C=
XM_005258764.1:c.*31C=	XP_005258821.1:n.*31C=
XM_006723148.1:c.*31C=	XP_006723211.1:n.*31C=
XM_011526754.1:c.*31C=	XP_011525056.1:n.*31C=
NM_000175.5:c.*31C= MANE Select	NP_000166.2:n.*31C=
NM_001289790.2:c.*31C=	NP_001276719.1:n.*31C=
NM_001329909.1:c.*31C=	NP_001316838.1:n.*31C=
NM_001329910.1:c.*31C=	NP_001316839.1:n.*31C=
NM_001329911.1:c.*31C=	NP_001316840.1:n.*31C=
XM_011526754.3:c.*31C=	XP_011525056.1:n.*31C=
NM_001289790.3:c.*31C=	NP_001276719.1:n.*31C=
NM_001329911.2:c.*31C=	NP_001316840.1:n.*31C=