Canonical Allele Identifier: CA2333167646

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34378971C= , CM000681.2:g.34378971C=	GRCh38
NC_000019.9:g.34869876C= , CM000681.1:g.34869876C=	GRCh37
NC_000019.8:g.39561716C=	NCBI36
NG_012838.2:g.19232C=
NG_012838.3:g.24380C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000175.5:c.671C= MANE Select	NP_000166.2:p.Thr224=
ENST00000356487.11:c.671C= MANE Select	ENSP00000348877.3:p.Thr224=
NM_000175.3:c.671C=	NP_000166.2:p.Thr224=
NM_001184722.1:c.704C=	NP_001171651.1:p.Thr235=
NM_001289789.1:c.788C=	NP_001276718.1:p.Thr263=
NM_001289790.1:c.587C=	NP_001276719.1:p.Thr196=
NM_001289790.2:c.587C=	NP_001276719.1:p.Thr196=
NM_001289790.3:c.587C=	NP_001276719.1:p.Thr196=
NM_001329909.1:c.671C=	NP_001316838.1:p.Thr224=
NM_001329910.1:c.671C=	NP_001316839.1:p.Thr224=
NM_001329911.1:c.671C=	NP_001316840.1:p.Thr224=
NM_001329911.2:c.671C=	NP_001316840.1:p.Thr224=
ENST00000356487.9:c.671C=	ENSP00000348877.3:p.Thr224=
ENST00000415930.7:c.704C=	ENSP00000405573.2:p.Thr235=
ENST00000415930.8:c.788C=	ENSP00000405573.3:p.Thr263=
ENST00000586425.1:c.671C=	ENSP00000467670.2:p.Thr224=
ENST00000586425.2:c.559C=
ENST00000588991.6:c.716C=	ENSP00000465858.2:p.Thr239=
ENST00000588991.7:c.704C=	ENSP00000465858.3:p.Thr235=
ENST00000589399.6:c.440C=	ENSP00000468201.2:p.Thr147=
ENST00000643067.1:n.1181C=
ENST00000647446.1:c.671C=	ENSP00000495129.1:p.Thr224=
XM_005258764.1:c.671C=	XP_005258821.1:p.Thr224=
XM_006723148.1:c.671C=	XP_006723211.1:p.Thr224=
XM_011526754.1:c.788C=	XP_011525056.1:p.Thr263=
XM_011526754.3:c.788C=	XP_011525056.1:p.Thr263=
XM_011526755.1:c.788C=	XP_011525057.1:p.Thr263=