Canonical Allele Identifier: CA2333177877
Gene: GPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.34399885C= , CM000681.2:g.34399885C= GRCh38
NC_000019.9:g.34890790C= , CM000681.1:g.34890790C= GRCh37
NC_000019.8:g.39582630C= NCBI36
NG_012838.2:g.40146C=
NG_012838.3:g.45294C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356487.11:c.1542-16C= MANE Select ENSP00000348877.3:n.1542-16C=
ENST00000415930.8:c.1659-16C= ENSP00000405573.3:n.1659-16C=
ENST00000586425.2:c.1208-16C=
ENST00000588991.7:c.1575-16C= ENSP00000465858.3:n.1575-16C=
ENST00000643067.1:n.2587-16C=
ENST00000647446.1:c.*593-16C= ENSP00000495129.1:n.*593-16C=
ENST00000356487.9:c.1542-16C= ENSP00000348877.3:n.1542-16C=
ENST00000415930.7:c.1575-16C= ENSP00000405573.2:n.1575-16C=
ENST00000586077.1:n.2603C=
ENST00000586392.1:n.1280-16C=
ENST00000586425.1:c.1399-16C= ENSP00000467670.2:n.1399-16C=
ENST00000588991.6:c.1587-16C= ENSP00000465858.2:n.1587-16C=
ENST00000592740.5:c.193+3228C=
NM_000175.3:c.1542-16C= NP_000166.2:n.1542-16C=
NM_001184722.1:c.1575-16C= NP_001171651.1:n.1575-16C=
NM_001289789.1:c.1659-16C= NP_001276718.1:n.1659-16C=
NM_001289790.1:c.1458-16C= NP_001276719.1:n.1458-16C=
XM_005258764.1:c.1542-16C= XP_005258821.1:n.1542-16C=
XM_006723148.1:c.1542-16C= XP_006723211.1:n.1542-16C=
XM_011526754.1:c.1659-16C= XP_011525056.1:n.1659-16C=
NM_000175.5:c.1542-16C= MANE Select NP_000166.2:n.1542-16C=
NM_001289790.2:c.1458-16C= NP_001276719.1:n.1458-16C=
NM_001329909.1:c.1542-16C= NP_001316838.1:n.1542-16C=
NM_001329910.1:c.1542-16C= NP_001316839.1:n.1542-16C=
NM_001329911.1:c.1515-16C= NP_001316840.1:n.1515-16C=
XM_011526754.3:c.1659-16C= XP_011525056.1:n.1659-16C=
NM_001289790.3:c.1458-16C= NP_001276719.1:n.1458-16C=
NM_001329911.2:c.1515-16C= NP_001316840.1:n.1515-16C=