Canonical Allele Identifier: CA2573156240

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34393776G>A , CM000681.2:g.34393776G>A	GRCh38
NC_000019.9:g.34884681G>A , CM000681.1:g.34884681G>A	GRCh37
NC_000019.8:g.39576521G>A	NCBI36
NG_012838.2:g.34037G>A
NG_012838.3:g.39185G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000175.5:c.909+5G>A MANE Select	NP_000166.2:n.909+5G>A
ENST00000356487.11:c.909+5G>A MANE Select	ENSP00000348877.3:n.909+5G>A
NM_000175.3:c.909+5G>A	NP_000166.2:n.909+5G>A
NM_001184722.1:c.942+5G>A	NP_001171651.1:n.942+5G>A
NM_001289789.1:c.1026+5G>A	NP_001276718.1:n.1026+5G>A
NM_001289790.1:c.825+5G>A	NP_001276719.1:n.825+5G>A
NM_001289790.2:c.825+5G>A	NP_001276719.1:n.825+5G>A
NM_001289790.3:c.825+5G>A	NP_001276719.1:n.825+5G>A
NM_001329909.1:c.909+5G>A	NP_001316838.1:n.909+5G>A
NM_001329910.1:c.909+5G>A	NP_001316839.1:n.909+5G>A
NM_001329911.1:c.909+5G>A	NP_001316840.1:n.909+5G>A
NM_001329911.2:c.909+5G>A	NP_001316840.1:n.909+5G>A
ENST00000356487.9:c.909+5G>A	ENSP00000348877.3:n.909+5G>A
ENST00000415930.7:c.942+5G>A	ENSP00000405573.2:n.942+5G>A
ENST00000415930.8:c.1026+5G>A	ENSP00000405573.3:n.1026+5G>A
ENST00000586392.1:n.510G>A
ENST00000586425.1:c.909+5G>A	ENSP00000467670.2:n.909+5G>A
ENST00000586425.2:c.797+5G>A
ENST00000588991.6:c.954+5G>A	ENSP00000465858.2:n.954+5G>A
ENST00000588991.7:c.942+5G>A	ENSP00000465858.3:n.942+5G>A
ENST00000589985.5:n.1157+5G>A
ENST00000643067.1:n.1954+5G>A
ENST00000647446.1:c.*37+5G>A	ENSP00000495129.1:n.*37+5G>A
XM_005258764.1:c.909+5G>A	XP_005258821.1:n.909+5G>A
XM_006723148.1:c.909+5G>A	XP_006723211.1:n.909+5G>A
XM_011526754.1:c.1026+5G>A	XP_011525056.1:n.1026+5G>A
XM_011526754.3:c.1026+5G>A	XP_011525056.1:n.1026+5G>A