Canonical Allele Identifier: CA9367323

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34394054G>A , CM000681.2:g.34394054G>A	GRCh38
NC_000019.9:g.34884959G>A , CM000681.1:g.34884959G>A	GRCh37
NC_000019.8:g.39576799G>A	NCBI36
NG_012838.2:g.34315G>A
NG_012838.3:g.39463G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1050G>A MANE Select	ENSP00000348877.3:p.Ala350=
ENST00000415930.8:c.1167G>A	ENSP00000405573.3:p.Ala389=
ENST00000586425.2:c.938G>A
ENST00000588991.7:c.1083G>A	ENSP00000465858.3:p.Ala361=
ENST00000643067.1:n.2095G>A
ENST00000647446.1:c.*178G>A	ENSP00000495129.1:n.*178G>A
ENST00000356487.9:c.1050G>A	ENSP00000348877.3:p.Ala350=
ENST00000415930.7:c.1083G>A	ENSP00000405573.2:p.Ala361=
ENST00000586392.1:n.788G>A
ENST00000586425.1:c.1050G>A	ENSP00000467670.2:p.Ala350=
ENST00000588991.6:c.1095G>A	ENSP00000465858.2:p.Ala365=
ENST00000589985.5:n.1298G>A
NM_000175.3:c.1050G>A	NP_000166.2:p.Ala350=
NM_001184722.1:c.1083G>A	NP_001171651.1:p.Ala361=
NM_001289789.1:c.1167G>A	NP_001276718.1:p.Ala389=
NM_001289790.1:c.966G>A	NP_001276719.1:p.Ala322=
XM_005258764.1:c.1050G>A	XP_005258821.1:p.Ala350=
XM_006723148.1:c.1050G>A	XP_006723211.1:p.Ala350=
XM_011526754.1:c.1167G>A	XP_011525056.1:p.Ala389=
NM_000175.5:c.1050G>A MANE Select	NP_000166.2:p.Ala350=
NM_001289790.2:c.966G>A	NP_001276719.1:p.Ala322=
NM_001329909.1:c.1050G>A	NP_001316838.1:p.Ala350=
NM_001329910.1:c.1050G>A	NP_001316839.1:p.Ala350=
NM_001329911.1:c.1050G>A	NP_001316840.1:p.Ala350=
XM_011526754.3:c.1167G>A	XP_011525056.1:p.Ala389=
NM_001289790.3:c.966G>A	NP_001276719.1:p.Ala322=
NM_001329911.2:c.1050G>A	NP_001316840.1:p.Ala350=