Canonical Allele Identifier: CA2531164148
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106467_1106468insGA , CM000681.2:g.1106467_1106468insGA GRCh38
NC_000019.9:g.1106466_1106467insGA , CM000681.1:g.1106466_1106467insGA GRCh37
NC_000019.8:g.1057466_1057467insGA NCBI36
NG_050621.1:g.7542_7543insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.672+8_672+9insGA ENSP00000473614.3:n.672+8_672+9insGA
ENST00000593032.6:c.541+8_541+9insGA ENSP00000465828.4:n.541+8_541+9insGA
ENST00000706713.1:c.555+8_555+9insGA ENSP00000516510.1:n.555+8_555+9insGA
ENST00000706714.1:c.541+8_541+9insGA ENSP00000516511.1:n.541+8_541+9insGA
ENST00000706715.1:c.177+8_177+9insGA ENSP00000516512.1:n.177+8_177+9insGA
ENST00000354171.13:c.561+8_561+9insGA MANE Select ENSP00000346103.7:n.561+8_561+9insGA
ENST00000589115.6:c.536+8_536+9insGA ENSP00000466872.3:n.536+8_536+9insGA
ENST00000354171.12:c.561+8_561+9insGA ENSP00000346103.7:n.561+8_561+9insGA
ENST00000585480.1:c.294+8_294+9insGA ENSP00000467900.1:n.294+8_294+9insGA
ENST00000587648.5:c.441+8_441+9insGA ENSP00000468349.1:n.441+8_441+9insGA
ENST00000588919.5:c.502+8_502+9insGA ENSP00000464989.3:n.502+8_502+9insGA
ENST00000589115.5:c.536+8_536+9insGA ENSP00000466872.2:n.536+8_536+9insGA
ENST00000592940.2:n.932+8_932+9insGA
ENST00000611653.4:c.480+8_480+9insGA ENSP00000483655.1:n.480+8_480+9insGA
ENST00000616066.4:c.558+8_558+9insGA ENSP00000485000.1:n.558+8_558+9insGA
ENST00000622390.4:c.669+8_669+9insGA ENSP00000477503.1:n.669+8_669+9insGA
NM_001039847.2:c.583+8_583+9insGA NP_001034936.1:n.583+8_583+9insGA
NM_001039848.2:c.672+8_672+9insGA NP_001034937.1:n.672+8_672+9insGA
NM_002085.4:c.561+8_561+9insGA NP_002076.2:n.561+8_561+9insGA
NM_001039848.3:c.672+8_672+9insGA NP_001034937.1:n.672+8_672+9insGA
NM_001039847.3:c.583+8_583+9insGA NP_001034936.1:n.583+8_583+9insGA
NM_001039848.4:c.672+8_672+9insGA NP_001034937.1:n.672+8_672+9insGA
NM_001367832.1:c.480+8_480+9insGA NP_001354761.1:n.480+8_480+9insGA
NM_002085.5:c.561+8_561+9insGA MANE Select NP_002076.2:n.561+8_561+9insGA