Canonical Allele Identifier: CA2588207186
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1105827_1105886del , CM000681.2:g.1105827_1105886del GRCh38
NC_000019.9:g.1105826_1105885del , CM000681.1:g.1105826_1105885del GRCh37
NC_000019.8:g.1056826_1056885del NCBI36
NG_050621.1:g.6902_6961del

Transcript Alleles

HGVS Amino-acid change
ENST00000585362.7:c.587+18_587+77del ENSP00000473614.3:n.587+18_587+77del
ENST00000593032.6:c.395+18_395+77del ENSP00000465828.4:n.395+18_395+77del
ENST00000706713.1:c.470+18_470+77del ENSP00000516510.1:n.470+18_470+77del
ENST00000706714.1:c.395+18_395+77del ENSP00000516511.1:n.395+18_395+77del
ENST00000706715.1:c.92+18_92+77del ENSP00000516512.1:n.92+18_92+77del
ENST00000354171.13:c.476+18_476+77del MANE Select ENSP00000346103.7:n.476+18_476+77del
ENST00000589115.6:c.476+18_476+77del ENSP00000466872.3:n.476+18_476+77del
ENST00000354171.12:c.476+18_476+77del ENSP00000346103.7:n.476+18_476+77del
ENST00000585480.1:c.209+18_209+77del ENSP00000467900.1:n.209+18_209+77del
ENST00000587648.5:c.356+18_356+77del ENSP00000468349.1:n.356+18_356+77del
ENST00000588919.5:c.395+18_395+77del ENSP00000464989.3:n.395+18_395+77del
ENST00000589115.5:c.476+18_476+77del ENSP00000466872.2:n.476+18_476+77del
ENST00000592940.2:n.433_492del
ENST00000593032.5:c.395+18_395+77del ENSP00000465828.3:n.395+18_395+77del
ENST00000611653.4:c.395+18_395+77del ENSP00000483655.1:n.395+18_395+77del
ENST00000616066.4:c.473+18_473+77del ENSP00000485000.1:n.473+18_473+77del
ENST00000622390.4:c.584+18_584+77del ENSP00000477503.1:n.584+18_584+77del
NM_001039847.2:c.476+18_476+77del NP_001034936.1:n.476+18_476+77del
NM_001039848.2:c.587+18_587+77del NP_001034937.1:n.587+18_587+77del
NM_002085.4:c.476+18_476+77del NP_002076.2:n.476+18_476+77del
NM_001039848.3:c.587+18_587+77del NP_001034937.1:n.587+18_587+77del
NM_001039847.3:c.476+18_476+77del NP_001034936.1:n.476+18_476+77del
NM_001039848.4:c.587+18_587+77del NP_001034937.1:n.587+18_587+77del
NM_001367832.1:c.395+18_395+77del NP_001354761.1:n.395+18_395+77del
NM_002085.5:c.476+18_476+77del MANE Select NP_002076.2:n.476+18_476+77del