Canonical Allele Identifier: CA645603782

Gene: GPX4

Linked Data

• COSMIC: COSM4447860

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106439_1106440delinsAA , CM000681.2:g.1106439_1106440delinsAA	GRCh38
NC_000019.9:g.1106438_1106439delinsAA , CM000681.1:g.1106438_1106439delinsAA	GRCh37
NC_000019.8:g.1057438_1057439delinsAA	NCBI36
NG_050621.1:g.7514_7515delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.652_653delinsAA	ENSP00000473614.3:p.Gly218Lys
ENST00000593032.6:c.521_522delinsAA	ENSP00000465828.4:p.Arg174Gln
ENST00000706713.1:c.535_536delinsAA	ENSP00000516510.1:p.Gly179Lys
ENST00000706714.1:c.521_522delinsAA	ENSP00000516511.1:p.Arg174Gln
ENST00000706715.1:c.157_158delinsAA	ENSP00000516512.1:p.Gly53Lys
ENST00000354171.13:c.541_542delinsAA MANE Select	ENSP00000346103.7:p.Gly181Lys
ENST00000589115.6:c.516_517delinsAA	ENSP00000466872.3:p.Asp173Asn
ENST00000354171.12:c.541_542delinsAA	ENSP00000346103.7:p.Gly181Lys
ENST00000585480.1:c.274_275delinsAA	ENSP00000467900.1:p.Gly92Lys
ENST00000587648.5:c.421_422delinsAA	ENSP00000468349.1:p.Gly141Lys
ENST00000588919.5:c.482_483delinsAA	ENSP00000464989.3:p.Arg161Gln
ENST00000589115.5:c.516_517delinsAA	ENSP00000466872.2:p.Asp173Asn
ENST00000592940.2:n.912_913delinsAA
ENST00000593032.5:c.521_522delinsAA	ENSP00000465828.3:p.Arg174Gln
ENST00000611653.4:c.460_461delinsAA	ENSP00000483655.1:p.Gly154Lys
ENST00000616066.4:c.538_539delinsAA	ENSP00000485000.1:p.Gly180Lys
ENST00000622390.4:c.649_650delinsAA	ENSP00000477503.1:p.Gly217Lys
NM_001039847.2:c.563_564delinsAA	NP_001034936.1:p.Arg188Gln
NM_001039848.2:c.652_653delinsAA	NP_001034937.1:p.Gly218Lys
NM_002085.4:c.541_542delinsAA	NP_002076.2:p.Gly181Lys
NM_001039848.3:c.652_653delinsAA	NP_001034937.1:p.Gly218Lys
NM_001039847.3:c.563_564delinsAA	NP_001034936.1:p.Arg188Gln
NM_001039848.4:c.652_653delinsAA	NP_001034937.1:p.Gly218Lys
NM_001367832.1:c.460_461delinsAA	NP_001354761.1:p.Gly154Lys
NM_002085.5:c.541_542delinsAA MANE Select	NP_002076.2:p.Gly181Lys