Canonical Allele Identifier: CA2333177893

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399935G= , CM000681.2:g.34399935G=	GRCh38
NC_000019.9:g.34890840G= , CM000681.1:g.34890840G=	GRCh37
NC_000019.8:g.39582680G=	NCBI36
NG_012838.2:g.40196G=
NG_012838.3:g.45344G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1576G= MANE Select	ENSP00000348877.3:p.Glu526=
ENST00000415930.8:c.1693G=	ENSP00000405573.3:p.Glu565=
ENST00000586425.2:c.1242G=
ENST00000588991.7:c.1609G=	ENSP00000465858.3:p.Glu537=
ENST00000643067.1:n.2621G=
ENST00000647446.1:c.*627G=	ENSP00000495129.1:n.*627G=
ENST00000356487.9:c.1576G=	ENSP00000348877.3:p.Glu526=
ENST00000415930.7:c.1609G=	ENSP00000405573.2:p.Glu537=
ENST00000586077.1:n.2653G=
ENST00000586392.1:n.1314G=
ENST00000586425.1:c.*8G=	ENSP00000467670.2:n.*8G=
ENST00000588991.6:c.1621G=	ENSP00000465858.2:p.Glu541=
ENST00000592740.5:c.193+3278G=
NM_000175.3:c.1576G=	NP_000166.2:p.Glu526=
NM_001184722.1:c.1609G=	NP_001171651.1:p.Glu537=
NM_001289789.1:c.1693G=	NP_001276718.1:p.Glu565=
NM_001289790.1:c.1492G=	NP_001276719.1:p.Glu498=
XM_005258764.1:c.1576G=	XP_005258821.1:p.Glu526=
XM_006723148.1:c.1576G=	XP_006723211.1:p.Glu526=
XM_011526754.1:c.1693G=	XP_011525056.1:p.Glu565=
NM_000175.5:c.1576G= MANE Select	NP_000166.2:p.Glu526=
NM_001289790.2:c.1492G=	NP_001276719.1:p.Glu498=
NM_001329909.1:c.1576G=	NP_001316838.1:p.Glu526=
NM_001329910.1:c.1576G=	NP_001316839.1:p.Glu526=
NM_001329911.1:c.1549G=	NP_001316840.1:p.Glu517=
XM_011526754.3:c.1693G=	XP_011525056.1:p.Glu565=
NM_001289790.3:c.1492G=	NP_001276719.1:p.Glu498=
NM_001329911.2:c.1549G=	NP_001316840.1:p.Glu517=