Canonical Allele Identifier: CA2333177941
Gene: GPI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.34400028_34400029delinsGT , CM000681.2:g.34400028_34400029delinsGT GRCh38
NC_000019.9:g.34890933_34890934delinsGT , CM000681.1:g.34890933_34890934delinsGT GRCh37
NC_000019.8:g.39582773_39582774delinsGT NCBI36
NG_012838.2:g.40289_40290delinsGT
NG_012838.3:g.45437_45438delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356487.11:c.1669_1670delinsGT MANE Select ENSP00000348877.3:p.Val557=
ENST00000415930.8:c.1786_1787delinsGT ENSP00000405573.3:p.Val596=
ENST00000586425.2:c.1335_1336delinsGT
ENST00000588991.7:c.1702_1703delinsGT ENSP00000465858.3:p.Val568=
ENST00000643067.1:n.2714_2715delinsGT
ENST00000647446.1:c.*720_*721delinsGT ENSP00000495129.1:n.*720_*721delinsGT
ENST00000356487.9:c.1669_1670delinsGT ENSP00000348877.3:p.Val557=
ENST00000415930.7:c.1702_1703delinsGT ENSP00000405573.2:p.Val568=
ENST00000586077.1:n.2746_2747delinsGT
ENST00000586392.1:n.1407_1408delinsGT
ENST00000586425.1:c.*101_*102delinsGT ENSP00000467670.2:n.*101_*102delinsGT
ENST00000588991.6:c.1714_1715delinsGT ENSP00000465858.2:p.Val572=
ENST00000592740.5:c.193+3371_193+3372delinsGT
NM_000175.3:c.1669_1670delinsGT NP_000166.2:p.Val557=
NM_001184722.1:c.1702_1703delinsGT NP_001171651.1:p.Val568=
NM_001289789.1:c.1786_1787delinsGT NP_001276718.1:p.Val596=
NM_001289790.1:c.1585_1586delinsGT NP_001276719.1:p.Val529=
XM_005258764.1:c.1669_1670delinsGT XP_005258821.1:p.Val557=
XM_006723148.1:c.1669_1670delinsGT XP_006723211.1:p.Val557=
XM_011526754.1:c.1786_1787delinsGT XP_011525056.1:p.Val596=
NM_000175.5:c.1669_1670delinsGT MANE Select NP_000166.2:p.Val557=
NM_001289790.2:c.1585_1586delinsGT NP_001276719.1:p.Val529=
NM_001329909.1:c.1669_1670delinsGT NP_001316838.1:p.Val557=
NM_001329910.1:c.1669_1670delinsGT NP_001316839.1:p.Val557=
NM_001329911.1:c.1642_1643delinsGT NP_001316840.1:p.Val548=
XM_011526754.3:c.1786_1787delinsGT XP_011525056.1:p.Val596=
NM_001289790.3:c.1585_1586delinsGT NP_001276719.1:p.Val529=
NM_001329911.2:c.1642_1643delinsGT NP_001316840.1:p.Val548=