Canonical Allele Identifier: CA2584357538

Gene: GPI

Linked Data

• gnomAD v4: 19-34400068-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.34400072del , CM000681.2:g.34400072del	GRCh38
NC_000019.9:g.34890977del , CM000681.1:g.34890977del	GRCh37
NC_000019.8:g.39582817del	NCBI36
NG_012838.2:g.40333del
NG_012838.3:g.45481del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356487.11:c.*36del MANE Select	ENSP00000348877.3:n.*36del
ENST00000415930.8:c.*36del	ENSP00000405573.3:n.*36del
ENST00000586425.2:c.1379del
ENST00000588991.7:c.*36del	ENSP00000465858.3:n.*36del
ENST00000643067.1:n.2758del
ENST00000647446.1:c.*764del	ENSP00000495129.1:n.*764del
ENST00000356487.9:c.*36del	ENSP00000348877.3:n.*36del
ENST00000415930.7:c.*36del	ENSP00000405573.2:n.*36del
ENST00000586077.1:n.2790del
ENST00000586392.1:n.1451del
ENST00000586425.1:c.*145del	ENSP00000467670.2:n.*145del
ENST00000588991.6:c.1758del	ENSP00000465858.2:n.1758del
ENST00000592740.5:c.193+3415del
NM_000175.3:c.*36del	NP_000166.2:n.*36del
NM_001184722.1:c.*36del	NP_001171651.1:n.*36del
NM_001289789.1:c.*36del	NP_001276718.1:n.*36del
NM_001289790.1:c.*36del	NP_001276719.1:n.*36del
XM_005258764.1:c.*36del	XP_005258821.1:n.*36del
XM_006723148.1:c.*36del	XP_006723211.1:n.*36del
XM_011526754.1:c.*36del	XP_011525056.1:n.*36del
NM_000175.5:c.*36del MANE Select	NP_000166.2:n.*36del
NM_001289790.2:c.*36del	NP_001276719.1:n.*36del
NM_001329909.1:c.*36del	NP_001316838.1:n.*36del
NM_001329910.1:c.*36del	NP_001316839.1:n.*36del
NM_001329911.1:c.*36del	NP_001316840.1:n.*36del
XM_011526754.3:c.*36del	XP_011525056.1:n.*36del
NM_001289790.3:c.*36del	NP_001276719.1:n.*36del
NM_001329911.2:c.*36del	NP_001316840.1:n.*36del