Canonical Allele Identifier: CA2333177752

Gene: GPI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399579C= , CM000681.2:g.34399579C=	GRCh38
NC_000019.9:g.34890484C= , CM000681.1:g.34890484C=	GRCh37
NC_000019.8:g.39582324C=	NCBI36
NG_012838.2:g.39840C=
NG_012838.3:g.44988C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1422C= MANE Select	ENSP00000348877.3:p.Thr474=
ENST00000415930.8:c.1539C=	ENSP00000405573.3:p.Thr513=
ENST00000586425.2:c.1158-157C=
ENST00000588991.7:c.1455C=	ENSP00000465858.3:p.Thr485=
ENST00000643067.1:n.2467C=
ENST00000647446.1:c.*473C=	ENSP00000495129.1:n.*473C=
ENST00000356487.9:c.1422C=	ENSP00000348877.3:p.Thr474=
ENST00000415930.7:c.1455C=	ENSP00000405573.2:p.Thr485=
ENST00000586077.1:n.2297C=
ENST00000586392.1:n.1160C=
ENST00000586425.1:c.1398+244C=	ENSP00000467670.2:n.1398+244C=
ENST00000588991.6:c.1467C=	ENSP00000465858.2:p.Thr489=
ENST00000592740.5:c.193+2922C=
NM_000175.3:c.1422C=	NP_000166.2:p.Thr474=
NM_001184722.1:c.1455C=	NP_001171651.1:p.Thr485=
NM_001289789.1:c.1539C=	NP_001276718.1:p.Thr513=
NM_001289790.1:c.1338C=	NP_001276719.1:p.Thr446=
XM_005258764.1:c.1422C=	XP_005258821.1:p.Thr474=
XM_006723148.1:c.1422C=	XP_006723211.1:p.Thr474=
XM_011526754.1:c.1539C=	XP_011525056.1:p.Thr513=
NM_000175.5:c.1422C= MANE Select	NP_000166.2:p.Thr474=
NM_001289790.2:c.1338C=	NP_001276719.1:p.Thr446=
NM_001329909.1:c.1422C=	NP_001316838.1:p.Thr474=
NM_001329910.1:c.1422C=	NP_001316839.1:p.Thr474=
NM_001329911.1:c.1395C=	NP_001316840.1:p.Thr465=
XM_011526754.3:c.1539C=	XP_011525056.1:p.Thr513=
NM_001289790.3:c.1338C=	NP_001276719.1:p.Thr446=
NM_001329911.2:c.1395C=	NP_001316840.1:p.Thr465=