Canonical Allele Identifier: CA2333177755

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399586A= , CM000681.2:g.34399586A=	GRCh38
NC_000019.9:g.34890491A= , CM000681.1:g.34890491A=	GRCh37
NC_000019.8:g.39582331A=	NCBI36
NG_012838.2:g.39847A=
NG_012838.3:g.44995A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1429A= MANE Select	ENSP00000348877.3:p.Ile477=
ENST00000415930.8:c.1546A=	ENSP00000405573.3:p.Ile516=
ENST00000586425.2:c.1158-150A=
ENST00000588991.7:c.1462A=	ENSP00000465858.3:p.Ile488=
ENST00000643067.1:n.2474A=
ENST00000647446.1:c.*480A=	ENSP00000495129.1:n.*480A=
ENST00000356487.9:c.1429A=	ENSP00000348877.3:p.Ile477=
ENST00000415930.7:c.1462A=	ENSP00000405573.2:p.Ile488=
ENST00000586077.1:n.2304A=
ENST00000586392.1:n.1167A=
ENST00000586425.1:c.1398+251A=	ENSP00000467670.2:n.1398+251A=
ENST00000588991.6:c.1474A=	ENSP00000465858.2:p.Ile492=
ENST00000592740.5:c.193+2929A=
NM_000175.3:c.1429A=	NP_000166.2:p.Ile477=
NM_001184722.1:c.1462A=	NP_001171651.1:p.Ile488=
NM_001289789.1:c.1546A=	NP_001276718.1:p.Ile516=
NM_001289790.1:c.1345A=	NP_001276719.1:p.Ile449=
XM_005258764.1:c.1429A=	XP_005258821.1:p.Ile477=
XM_006723148.1:c.1429A=	XP_006723211.1:p.Ile477=
XM_011526754.1:c.1546A=	XP_011525056.1:p.Ile516=
NM_000175.5:c.1429A= MANE Select	NP_000166.2:p.Ile477=
NM_001289790.2:c.1345A=	NP_001276719.1:p.Ile449=
NM_001329909.1:c.1429A=	NP_001316838.1:p.Ile477=
NM_001329910.1:c.1429A=	NP_001316839.1:p.Ile477=
NM_001329911.1:c.1402A=	NP_001316840.1:p.Ile468=
XM_011526754.3:c.1546A=	XP_011525056.1:p.Ile516=
NM_001289790.3:c.1345A=	NP_001276719.1:p.Ile449=
NM_001329911.2:c.1402A=	NP_001316840.1:p.Ile468=