Canonical Allele Identifier: CA2333177750

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399577A= , CM000681.2:g.34399577A=	GRCh38
NC_000019.9:g.34890482A= , CM000681.1:g.34890482A=	GRCh37
NC_000019.8:g.39582322A=	NCBI36
NG_012838.2:g.39838A=
NG_012838.3:g.44986A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1420A= MANE Select	ENSP00000348877.3:p.Thr474=
ENST00000415930.8:c.1537A=	ENSP00000405573.3:p.Thr513=
ENST00000586425.2:c.1158-159A=
ENST00000588991.7:c.1453A=	ENSP00000465858.3:p.Thr485=
ENST00000643067.1:n.2465A=
ENST00000647446.1:c.*471A=	ENSP00000495129.1:n.*471A=
ENST00000356487.9:c.1420A=	ENSP00000348877.3:p.Thr474=
ENST00000415930.7:c.1453A=	ENSP00000405573.2:p.Thr485=
ENST00000586077.1:n.2295A=
ENST00000586392.1:n.1158A=
ENST00000586425.1:c.1398+242A=	ENSP00000467670.2:n.1398+242A=
ENST00000588991.6:c.1465A=	ENSP00000465858.2:p.Thr489=
ENST00000592740.5:c.193+2920A=
NM_000175.3:c.1420A=	NP_000166.2:p.Thr474=
NM_001184722.1:c.1453A=	NP_001171651.1:p.Thr485=
NM_001289789.1:c.1537A=	NP_001276718.1:p.Thr513=
NM_001289790.1:c.1336A=	NP_001276719.1:p.Thr446=
XM_005258764.1:c.1420A=	XP_005258821.1:p.Thr474=
XM_006723148.1:c.1420A=	XP_006723211.1:p.Thr474=
XM_011526754.1:c.1537A=	XP_011525056.1:p.Thr513=
NM_000175.5:c.1420A= MANE Select	NP_000166.2:p.Thr474=
NM_001289790.2:c.1336A=	NP_001276719.1:p.Thr446=
NM_001329909.1:c.1420A=	NP_001316838.1:p.Thr474=
NM_001329910.1:c.1420A=	NP_001316839.1:p.Thr474=
NM_001329911.1:c.1393A=	NP_001316840.1:p.Thr465=
XM_011526754.3:c.1537A=	XP_011525056.1:p.Thr513=
NM_001289790.3:c.1336A=	NP_001276719.1:p.Thr446=
NM_001329911.2:c.1393A=	NP_001316840.1:p.Thr465=