Canonical Allele Identifier: CA9037466
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs369851110
gnomAD v2: 19-1106408-G-A
gnomAD v3: 19-1106409-G-A
gnomAD v4: 19-1106409-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106409G>A , CM000681.2:g.1106409G>A GRCh38
NC_000019.9:g.1106408G>A , CM000681.1:g.1106408G>A GRCh37
NC_000019.8:g.1057408G>A NCBI36
NG_050621.1:g.7484G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.622G>A ENSP00000473614.3:p.Asp208Asn
ENST00000593032.6:c.491G>A ENSP00000465828.4:p.Arg164Gln
ENST00000706713.1:c.505G>A ENSP00000516510.1:p.Asp169Asn
ENST00000706714.1:c.491G>A ENSP00000516511.1:p.Arg164Gln
ENST00000706715.1:c.127G>A ENSP00000516512.1:p.Asp43Asn
ENST00000354171.13:c.511G>A MANE Select ENSP00000346103.7:p.Asp171Asn
ENST00000589115.6:c.486G>A ENSP00000466872.3:p.Ser162=
ENST00000354171.12:c.511G>A ENSP00000346103.7:p.Asp171Asn
ENST00000585480.1:c.244G>A ENSP00000467900.1:p.Asp82Asn
ENST00000587648.5:c.391G>A ENSP00000468349.1:p.Asp131Asn
ENST00000588919.5:c.452G>A ENSP00000464989.3:p.Arg151Gln
ENST00000589115.5:c.486G>A ENSP00000466872.2:p.Ser162=
ENST00000592940.2:n.882G>A
ENST00000593032.5:c.491G>A ENSP00000465828.3:p.Arg164Gln
ENST00000611653.4:c.430G>A ENSP00000483655.1:p.Asp144Asn
ENST00000616066.4:c.508G>A ENSP00000485000.1:p.Asp170Asn
ENST00000622390.4:c.619G>A ENSP00000477503.1:p.Asp207Asn
NM_001039847.2:c.533G>A NP_001034936.1:p.Arg178Gln
NM_001039848.2:c.622G>A NP_001034937.1:p.Asp208Asn
NM_002085.4:c.511G>A NP_002076.2:p.Asp171Asn
NM_001039848.3:c.622G>A NP_001034937.1:p.Asp208Asn
NM_001039847.3:c.533G>A NP_001034936.1:p.Arg178Gln
NM_001039848.4:c.622G>A NP_001034937.1:p.Asp208Asn
NM_001367832.1:c.430G>A NP_001354761.1:p.Asp144Asn
NM_002085.5:c.511G>A MANE Select NP_002076.2:p.Asp171Asn