Canonical Allele Identifier: CA2333167591

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34378879A= , CM000681.2:g.34378879A=	GRCh38
NC_000019.9:g.34869784A= , CM000681.1:g.34869784A=	GRCh37
NC_000019.8:g.39561624A=	NCBI36
NG_012838.2:g.19140A=
NG_012838.3:g.24288A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.634-55A= MANE Select	ENSP00000348877.3:n.634-55A=
ENST00000415930.8:c.751-55A=	ENSP00000405573.3:n.751-55A=
ENST00000586425.2:c.522-55A=
ENST00000588991.7:c.667-55A=	ENSP00000465858.3:n.667-55A=
ENST00000589399.6:c.403-55A=	ENSP00000468201.2:n.403-55A=
ENST00000643067.1:n.1144-55A=
ENST00000647446.1:c.634-55A=	ENSP00000495129.1:n.634-55A=
ENST00000356487.9:c.634-55A=	ENSP00000348877.3:n.634-55A=
ENST00000415930.7:c.667-55A=	ENSP00000405573.2:n.667-55A=
ENST00000586425.1:c.634-55A=	ENSP00000467670.2:n.634-55A=
ENST00000588991.6:c.679-55A=	ENSP00000465858.2:n.679-55A=
NM_000175.3:c.634-55A=	NP_000166.2:n.634-55A=
NM_001184722.1:c.667-55A=	NP_001171651.1:n.667-55A=
NM_001289789.1:c.751-55A=	NP_001276718.1:n.751-55A=
NM_001289790.1:c.550-55A=	NP_001276719.1:n.550-55A=
XM_005258764.1:c.634-55A=	XP_005258821.1:n.634-55A=
XM_006723148.1:c.634-55A=	XP_006723211.1:n.634-55A=
XM_011526754.1:c.751-55A=	XP_011525056.1:n.751-55A=
XM_011526755.1:c.751-55A=	XP_011525057.1:n.751-55A=
NM_000175.5:c.634-55A= MANE Select	NP_000166.2:n.634-55A=
NM_001289790.2:c.550-55A=	NP_001276719.1:n.550-55A=
NM_001329909.1:c.634-55A=	NP_001316838.1:n.634-55A=
NM_001329910.1:c.634-55A=	NP_001316839.1:n.634-55A=
NM_001329911.1:c.634-55A=	NP_001316840.1:n.634-55A=
XM_011526754.3:c.751-55A=	XP_011525056.1:n.751-55A=
NM_001289790.3:c.550-55A=	NP_001276719.1:n.550-55A=
NM_001329911.2:c.634-55A=	NP_001316840.1:n.634-55A=