Canonical Allele Identifier: CA2333177952

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400054G= , CM000681.2:g.34400054G=	GRCh38
NC_000019.9:g.34890959G= , CM000681.1:g.34890959G=	GRCh37
NC_000019.8:g.39582799G=	NCBI36
NG_012838.2:g.40315G=
NG_012838.3:g.45463G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.*18G= MANE Select	ENSP00000348877.3:n.*18G=
ENST00000415930.8:c.*18G=	ENSP00000405573.3:n.*18G=
ENST00000586425.2:c.1361G=
ENST00000588991.7:c.*18G=	ENSP00000465858.3:n.*18G=
ENST00000643067.1:n.2740G=
ENST00000647446.1:c.*746G=	ENSP00000495129.1:n.*746G=
ENST00000356487.9:c.*18G=	ENSP00000348877.3:n.*18G=
ENST00000415930.7:c.*18G=	ENSP00000405573.2:n.*18G=
ENST00000586077.1:n.2772G=
ENST00000586392.1:n.1433G=
ENST00000586425.1:c.*127G=	ENSP00000467670.2:n.*127G=
ENST00000588991.6:c.1740G=	ENSP00000465858.2:n.1740G=
ENST00000592740.5:c.193+3397G=
NM_000175.3:c.*18G=	NP_000166.2:n.*18G=
NM_001184722.1:c.*18G=	NP_001171651.1:n.*18G=
NM_001289789.1:c.*18G=	NP_001276718.1:n.*18G=
NM_001289790.1:c.*18G=	NP_001276719.1:n.*18G=
XM_005258764.1:c.*18G=	XP_005258821.1:n.*18G=
XM_006723148.1:c.*18G=	XP_006723211.1:n.*18G=
XM_011526754.1:c.*18G=	XP_011525056.1:n.*18G=
NM_000175.5:c.*18G= MANE Select	NP_000166.2:n.*18G=
NM_001289790.2:c.*18G=	NP_001276719.1:n.*18G=
NM_001329909.1:c.*18G=	NP_001316838.1:n.*18G=
NM_001329910.1:c.*18G=	NP_001316839.1:n.*18G=
NM_001329911.1:c.*18G=	NP_001316840.1:n.*18G=
XM_011526754.3:c.*18G=	XP_011525056.1:n.*18G=
NM_001289790.3:c.*18G=	NP_001276719.1:n.*18G=
NM_001329911.2:c.*18G=	NP_001316840.1:n.*18G=