Canonical Allele Identifier: CA2333177892

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399933T= , CM000681.2:g.34399933T=	GRCh38
NC_000019.9:g.34890838T= , CM000681.1:g.34890838T=	GRCh37
NC_000019.8:g.39582678T=	NCBI36
NG_012838.2:g.40194T=
NG_012838.3:g.45342T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1574T= MANE Select	ENSP00000348877.3:p.Ile525=
ENST00000415930.8:c.1691T=	ENSP00000405573.3:p.Ile564=
ENST00000586425.2:c.1240T=
ENST00000588991.7:c.1607T=	ENSP00000465858.3:p.Ile536=
ENST00000643067.1:n.2619T=
ENST00000647446.1:c.*625T=	ENSP00000495129.1:n.*625T=
ENST00000356487.9:c.1574T=	ENSP00000348877.3:p.Ile525=
ENST00000415930.7:c.1607T=	ENSP00000405573.2:p.Ile536=
ENST00000586077.1:n.2651T=
ENST00000586392.1:n.1312T=
ENST00000586425.1:c.*6T=	ENSP00000467670.2:n.*6T=
ENST00000588991.6:c.1619T=	ENSP00000465858.2:p.Ile540=
ENST00000592740.5:c.193+3276T=
NM_000175.3:c.1574T=	NP_000166.2:p.Ile525=
NM_001184722.1:c.1607T=	NP_001171651.1:p.Ile536=
NM_001289789.1:c.1691T=	NP_001276718.1:p.Ile564=
NM_001289790.1:c.1490T=	NP_001276719.1:p.Ile497=
XM_005258764.1:c.1574T=	XP_005258821.1:p.Ile525=
XM_006723148.1:c.1574T=	XP_006723211.1:p.Ile525=
XM_011526754.1:c.1691T=	XP_011525056.1:p.Ile564=
NM_000175.5:c.1574T= MANE Select	NP_000166.2:p.Ile525=
NM_001289790.2:c.1490T=	NP_001276719.1:p.Ile497=
NM_001329909.1:c.1574T=	NP_001316838.1:p.Ile525=
NM_001329910.1:c.1574T=	NP_001316839.1:p.Ile525=
NM_001329911.1:c.1547T=	NP_001316840.1:p.Ile516=
XM_011526754.3:c.1691T=	XP_011525056.1:p.Ile564=
NM_001289790.3:c.1490T=	NP_001276719.1:p.Ile497=
NM_001329911.2:c.1547T=	NP_001316840.1:p.Ile516=