Canonical Allele Identifier: CA405246639
Gene: GPI HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.34399931A>T , CM000681.2:g.34399931A>T GRCh38
NC_000019.9:g.34890836A>T , CM000681.1:g.34890836A>T GRCh37
NC_000019.8:g.39582676A>T NCBI36
NG_012838.2:g.40192A>T
NG_012838.3:g.45340A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356487.11:c.1572A>T MANE Select ENSP00000348877.3:p.Lys524Asn
ENST00000415930.8:c.1689A>T ENSP00000405573.3:p.Lys563Asn
ENST00000586425.2:c.1238A>T
ENST00000588991.7:c.1605A>T ENSP00000465858.3:p.Lys535Asn
ENST00000643067.1:n.2617A>T
ENST00000647446.1:c.*623A>T ENSP00000495129.1:n.*623A>T
ENST00000356487.9:c.1572A>T ENSP00000348877.3:p.Lys524Asn
ENST00000415930.7:c.1605A>T ENSP00000405573.2:p.Lys535Asn
ENST00000586077.1:n.2649A>T
ENST00000586392.1:n.1310A>T
ENST00000586425.1:c.*4A>T ENSP00000467670.2:n.*4A>T
ENST00000588991.6:c.1617A>T ENSP00000465858.2:p.Lys539Asn
ENST00000592740.5:c.193+3274A>T
NM_000175.3:c.1572A>T NP_000166.2:p.Lys524Asn
NM_001184722.1:c.1605A>T NP_001171651.1:p.Lys535Asn
NM_001289789.1:c.1689A>T NP_001276718.1:p.Lys563Asn
NM_001289790.1:c.1488A>T NP_001276719.1:p.Lys496Asn
XM_005258764.1:c.1572A>T XP_005258821.1:p.Lys524Asn
XM_006723148.1:c.1572A>T XP_006723211.1:p.Lys524Asn
XM_011526754.1:c.1689A>T XP_011525056.1:p.Lys563Asn
NM_000175.5:c.1572A>T MANE Select NP_000166.2:p.Lys524Asn
NM_001289790.2:c.1488A>T NP_001276719.1:p.Lys496Asn
NM_001329909.1:c.1572A>T NP_001316838.1:p.Lys524Asn
NM_001329910.1:c.1572A>T NP_001316839.1:p.Lys524Asn
NM_001329911.1:c.1545A>T NP_001316840.1:p.Lys515Asn
XM_011526754.3:c.1689A>T XP_011525056.1:p.Lys563Asn
NM_001289790.3:c.1488A>T NP_001276719.1:p.Lys496Asn
NM_001329911.2:c.1545A>T NP_001316840.1:p.Lys515Asn