Canonical Allele Identifier: CA2588207227
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1105845_1105866del , CM000681.2:g.1105845_1105866del GRCh38
NC_000019.9:g.1105844_1105865del , CM000681.1:g.1105844_1105865del GRCh37
NC_000019.8:g.1056844_1056865del NCBI36
NG_050621.1:g.6920_6941del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.587+36_587+57del ENSP00000473614.3:n.587+36_587+57del
ENST00000593032.6:c.395+36_395+57del ENSP00000465828.4:n.395+36_395+57del
ENST00000706713.1:c.470+36_470+57del ENSP00000516510.1:n.470+36_470+57del
ENST00000706714.1:c.395+36_395+57del ENSP00000516511.1:n.395+36_395+57del
ENST00000706715.1:c.92+36_92+57del ENSP00000516512.1:n.92+36_92+57del
ENST00000354171.13:c.476+36_476+57del MANE Select ENSP00000346103.7:n.476+36_476+57del
ENST00000589115.6:c.476+36_476+57del ENSP00000466872.3:n.476+36_476+57del
ENST00000354171.12:c.476+36_476+57del ENSP00000346103.7:n.476+36_476+57del
ENST00000585480.1:c.209+36_209+57del ENSP00000467900.1:n.209+36_209+57del
ENST00000587648.5:c.356+36_356+57del ENSP00000468349.1:n.356+36_356+57del
ENST00000588919.5:c.395+36_395+57del ENSP00000464989.3:n.395+36_395+57del
ENST00000589115.5:c.476+36_476+57del ENSP00000466872.2:n.476+36_476+57del
ENST00000592940.2:n.451_472del
ENST00000593032.5:c.395+36_395+57del ENSP00000465828.3:n.395+36_395+57del
ENST00000611653.4:c.395+36_395+57del ENSP00000483655.1:n.395+36_395+57del
ENST00000616066.4:c.473+36_473+57del ENSP00000485000.1:n.473+36_473+57del
ENST00000622390.4:c.584+36_584+57del ENSP00000477503.1:n.584+36_584+57del
NM_001039847.2:c.476+36_476+57del NP_001034936.1:n.476+36_476+57del
NM_001039848.2:c.587+36_587+57del NP_001034937.1:n.587+36_587+57del
NM_002085.4:c.476+36_476+57del NP_002076.2:n.476+36_476+57del
NM_001039848.3:c.587+36_587+57del NP_001034937.1:n.587+36_587+57del
NM_001039847.3:c.476+36_476+57del NP_001034936.1:n.476+36_476+57del
NM_001039848.4:c.587+36_587+57del NP_001034937.1:n.587+36_587+57del
NM_001367832.1:c.395+36_395+57del NP_001354761.1:n.395+36_395+57del
NM_002085.5:c.476+36_476+57del MANE Select NP_002076.2:n.476+36_476+57del