Canonical Allele Identifier: CA2317520658
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106431A= , CM000681.2:g.1106431A= GRCh38
NC_000019.9:g.1106430A= , CM000681.1:g.1106430A= GRCh37
NC_000019.8:g.1057430A= NCBI36
NG_050621.1:g.7506A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.644A= ENSP00000473614.3:p.Lys215=
ENST00000593032.6:c.513A= ENSP00000465828.4:p.Glu171=
ENST00000706713.1:c.527A= ENSP00000516510.1:p.Lys176=
ENST00000706714.1:c.513A= ENSP00000516511.1:p.Glu171=
ENST00000706715.1:c.149A= ENSP00000516512.1:p.Lys50=
ENST00000354171.13:c.533A= MANE Select ENSP00000346103.7:p.Lys178=
ENST00000589115.6:c.508A= ENSP00000466872.3:p.Ser170=
ENST00000354171.12:c.533A= ENSP00000346103.7:p.Lys178=
ENST00000585480.1:c.266A= ENSP00000467900.1:p.Lys89=
ENST00000587648.5:c.413A= ENSP00000468349.1:p.Lys138=
ENST00000588919.5:c.474A= ENSP00000464989.3:p.Glu158=
ENST00000589115.5:c.508A= ENSP00000466872.2:p.Ser170=
ENST00000592940.2:n.904A=
ENST00000593032.5:c.513A= ENSP00000465828.3:p.Glu171=
ENST00000611653.4:c.452A= ENSP00000483655.1:p.Lys151=
ENST00000616066.4:c.530A= ENSP00000485000.1:p.Lys177=
ENST00000622390.4:c.641A= ENSP00000477503.1:p.Lys214=
NM_001039847.2:c.555A= NP_001034936.1:p.Glu185=
NM_001039848.2:c.644A= NP_001034937.1:p.Lys215=
NM_002085.4:c.533A= NP_002076.2:p.Lys178=
NM_001039848.3:c.644A= NP_001034937.1:p.Lys215=
NM_001039847.3:c.555A= NP_001034936.1:p.Glu185=
NM_001039848.4:c.644A= NP_001034937.1:p.Lys215=
NM_001367832.1:c.452A= NP_001354761.1:p.Lys151=
NM_002085.5:c.533A= MANE Select NP_002076.2:p.Lys178=