Canonical Allele Identifier: CA2584357472

Gene: GPI

Linked Data

• gnomAD v4: 19-34399606-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34399608del , CM000681.2:g.34399608del	GRCh38
NC_000019.9:g.34890513del , CM000681.1:g.34890513del	GRCh37
NC_000019.8:g.39582353del	NCBI36
NG_012838.2:g.39869del
NG_012838.3:g.45017del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.1451del MANE Select	ENSP00000348877.3:p.Pro484HisfsTer?
ENST00000415930.8:c.1568del	ENSP00000405573.3:p.Pro523HisfsTer?
ENST00000586425.2:c.1158-128del
ENST00000588991.7:c.1484del	ENSP00000465858.3:p.Pro495HisfsTer?
ENST00000643067.1:n.2496del
ENST00000647446.1:c.*502del	ENSP00000495129.1:n.*502del
ENST00000356487.9:c.1451del	ENSP00000348877.3:p.Pro484HisfsTer?
ENST00000415930.7:c.1484del	ENSP00000405573.2:p.Pro495HisfsTer?
ENST00000586077.1:n.2326del
ENST00000586392.1:n.1189del
ENST00000586425.1:c.1398+273del	ENSP00000467670.2:n.1398+273del
ENST00000588991.6:c.1496del	ENSP00000465858.2:p.Pro499HisfsTer?
ENST00000592740.5:c.193+2951del
NM_000175.3:c.1451del	NP_000166.2:p.Pro484HisfsTer?
NM_001184722.1:c.1484del	NP_001171651.1:p.Pro495HisfsTer?
NM_001289789.1:c.1568del	NP_001276718.1:p.Pro523HisfsTer?
NM_001289790.1:c.1367del	NP_001276719.1:p.Pro456HisfsTer?
XM_005258764.1:c.1451del	XP_005258821.1:p.Pro484HisfsTer?
XM_006723148.1:c.1451del	XP_006723211.1:p.Pro484HisfsTer?
XM_011526754.1:c.1568del	XP_011525056.1:p.Pro523HisfsTer?
NM_000175.5:c.1451del MANE Select	NP_000166.2:p.Pro484HisfsTer?
NM_001289790.2:c.1367del	NP_001276719.1:p.Pro456HisfsTer?
NM_001329909.1:c.1451del	NP_001316838.1:p.Pro484HisfsTer?
NM_001329910.1:c.1451del	NP_001316839.1:p.Pro484HisfsTer?
NM_001329911.1:c.1424del	NP_001316840.1:p.Pro475HisfsTer?
XM_011526754.3:c.1568del	XP_011525056.1:p.Pro523HisfsTer?
NM_001289790.3:c.1367del	NP_001276719.1:p.Pro456HisfsTer?
NM_001329911.2:c.1424del	NP_001316840.1:p.Pro475HisfsTer?