Canonical Allele Identifier: CA2333177891

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399927A= , CM000681.2:g.34399927A=	GRCh38
NC_000019.9:g.34890832A= , CM000681.1:g.34890832A=	GRCh37
NC_000019.8:g.39582672A=	NCBI36
NG_012838.2:g.40188A=
NG_012838.3:g.45336A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1568A= MANE Select	ENSP00000348877.3:p.Lys523=
ENST00000415930.8:c.1685A=	ENSP00000405573.3:p.Lys562=
ENST00000586425.2:c.1234A=
ENST00000588991.7:c.1601A=	ENSP00000465858.3:p.Lys534=
ENST00000643067.1:n.2613A=
ENST00000647446.1:c.*619A=	ENSP00000495129.1:n.*619A=
ENST00000356487.9:c.1568A=	ENSP00000348877.3:p.Lys523=
ENST00000415930.7:c.1601A=	ENSP00000405573.2:p.Lys534=
ENST00000586077.1:n.2645A=
ENST00000586392.1:n.1306A=
ENST00000586425.1:c.1425A=	ENSP00000467670.2:p.Ter475=
ENST00000588991.6:c.1613A=	ENSP00000465858.2:p.Lys538=
ENST00000592740.5:c.193+3270A=
NM_000175.3:c.1568A=	NP_000166.2:p.Lys523=
NM_001184722.1:c.1601A=	NP_001171651.1:p.Lys534=
NM_001289789.1:c.1685A=	NP_001276718.1:p.Lys562=
NM_001289790.1:c.1484A=	NP_001276719.1:p.Lys495=
XM_005258764.1:c.1568A=	XP_005258821.1:p.Lys523=
XM_006723148.1:c.1568A=	XP_006723211.1:p.Lys523=
XM_011526754.1:c.1685A=	XP_011525056.1:p.Lys562=
NM_000175.5:c.1568A= MANE Select	NP_000166.2:p.Lys523=
NM_001289790.2:c.1484A=	NP_001276719.1:p.Lys495=
NM_001329909.1:c.1568A=	NP_001316838.1:p.Lys523=
NM_001329910.1:c.1568A=	NP_001316839.1:p.Lys523=
NM_001329911.1:c.1541A=	NP_001316840.1:p.Lys514=
XM_011526754.3:c.1685A=	XP_011525056.1:p.Lys562=
NM_001289790.3:c.1484A=	NP_001276719.1:p.Lys495=
NM_001329911.2:c.1541A=	NP_001316840.1:p.Lys514=