Canonical Allele Identifier: CA2333177849

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399825T= , CM000681.2:g.34399825T=	GRCh38
NC_000019.9:g.34890730T= , CM000681.1:g.34890730T=	GRCh37
NC_000019.8:g.39582570T=	NCBI36
NG_012838.2:g.40086T=
NG_012838.3:g.45234T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1541+40T= MANE Select	ENSP00000348877.3:n.1541+40T=
ENST00000415930.8:c.1658+40T=	ENSP00000405573.3:n.1658+40T=
ENST00000586425.2:c.1207+40T=
ENST00000588991.7:c.1574+40T=	ENSP00000465858.3:n.1574+40T=
ENST00000643067.1:n.2586+40T=
ENST00000647446.1:c.*592+40T=	ENSP00000495129.1:n.*592+40T=
ENST00000356487.9:c.1541+40T=	ENSP00000348877.3:n.1541+40T=
ENST00000415930.7:c.1574+40T=	ENSP00000405573.2:n.1574+40T=
ENST00000586077.1:n.2543T=
ENST00000586392.1:n.1279+40T=
ENST00000586425.1:c.1399-76T=	ENSP00000467670.2:n.1399-76T=
ENST00000588991.6:c.1586+40T=	ENSP00000465858.2:n.1586+40T=
ENST00000592740.5:c.193+3168T=
NM_000175.3:c.1541+40T=	NP_000166.2:n.1541+40T=
NM_001184722.1:c.1574+40T=	NP_001171651.1:n.1574+40T=
NM_001289789.1:c.1658+40T=	NP_001276718.1:n.1658+40T=
NM_001289790.1:c.1457+40T=	NP_001276719.1:n.1457+40T=
XM_005258764.1:c.1541+40T=	XP_005258821.1:n.1541+40T=
XM_006723148.1:c.1541+40T=	XP_006723211.1:n.1541+40T=
XM_011526754.1:c.1658+40T=	XP_011525056.1:n.1658+40T=
NM_000175.5:c.1541+40T= MANE Select	NP_000166.2:n.1541+40T=
NM_001289790.2:c.1457+40T=	NP_001276719.1:n.1457+40T=
NM_001329909.1:c.1541+40T=	NP_001316838.1:n.1541+40T=
NM_001329910.1:c.1541+40T=	NP_001316839.1:n.1541+40T=
NM_001329911.1:c.1514+40T=	NP_001316840.1:n.1514+40T=
XM_011526754.3:c.1658+40T=	XP_011525056.1:n.1658+40T=
NM_001289790.3:c.1457+40T=	NP_001276719.1:n.1457+40T=
NM_001329911.2:c.1514+40T=	NP_001316840.1:n.1514+40T=