Canonical Allele Identifier: CA2333177944

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400033A= , CM000681.2:g.34400033A=	GRCh38
NC_000019.9:g.34890938A= , CM000681.1:g.34890938A=	GRCh37
NC_000019.8:g.39582778A=	NCBI36
NG_012838.2:g.40294A=
NG_012838.3:g.45442A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1674A= MANE Select	ENSP00000348877.3:p.Gln558=
ENST00000415930.8:c.1791A=	ENSP00000405573.3:p.Gln597=
ENST00000586425.2:c.1340A=
ENST00000588991.7:c.1707A=	ENSP00000465858.3:p.Gln569=
ENST00000643067.1:n.2719A=
ENST00000647446.1:c.*725A=	ENSP00000495129.1:n.*725A=
ENST00000356487.9:c.1674A=	ENSP00000348877.3:p.Gln558=
ENST00000415930.7:c.1707A=	ENSP00000405573.2:p.Gln569=
ENST00000586077.1:n.2751A=
ENST00000586392.1:n.1412A=
ENST00000586425.1:c.*106A=	ENSP00000467670.2:n.*106A=
ENST00000588991.6:c.1719A=	ENSP00000465858.2:p.Gln573=
ENST00000592740.5:c.193+3376A=
NM_000175.3:c.1674A=	NP_000166.2:p.Gln558=
NM_001184722.1:c.1707A=	NP_001171651.1:p.Gln569=
NM_001289789.1:c.1791A=	NP_001276718.1:p.Gln597=
NM_001289790.1:c.1590A=	NP_001276719.1:p.Gln530=
XM_005258764.1:c.1674A=	XP_005258821.1:p.Gln558=
XM_006723148.1:c.1674A=	XP_006723211.1:p.Gln558=
XM_011526754.1:c.1791A=	XP_011525056.1:p.Gln597=
NM_000175.5:c.1674A= MANE Select	NP_000166.2:p.Gln558=
NM_001289790.2:c.1590A=	NP_001276719.1:p.Gln530=
NM_001329909.1:c.1674A=	NP_001316838.1:p.Gln558=
NM_001329910.1:c.1674A=	NP_001316839.1:p.Gln558=
NM_001329911.1:c.1647A=	NP_001316840.1:p.Gln549=
XM_011526754.3:c.1791A=	XP_011525056.1:p.Gln597=
NM_001289790.3:c.1590A=	NP_001276719.1:p.Gln530=
NM_001329911.2:c.1647A=	NP_001316840.1:p.Gln549=