Canonical Allele Identifier: CA2317520112
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1105735C= , CM000681.2:g.1105735C= GRCh38
NC_000019.9:g.1105734C= , CM000681.1:g.1105734C= GRCh37
NC_000019.8:g.1056734C= NCBI36
NG_050621.1:g.6810C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.513C= ENSP00000473614.3:p.Cys171=
ENST00000593032.6:c.321C= ENSP00000465828.4:p.Cys107=
ENST00000706713.1:c.396C= ENSP00000516510.1:p.Cys132=
ENST00000706714.1:c.321C= ENSP00000516511.1:p.Cys107=
ENST00000706715.1:c.18C= ENSP00000516512.1:p.Cys6=
ENST00000354171.13:c.402C= MANE Select ENSP00000346103.7:p.Cys134=
ENST00000589115.6:c.402C= ENSP00000466872.3:p.Cys134=
ENST00000354171.12:c.402C= ENSP00000346103.7:p.Cys134=
ENST00000585362.6:c.513C= ENSP00000473614.2:p.Cys171=
ENST00000585480.1:c.135C= ENSP00000467900.1:p.Cys45=
ENST00000587648.5:c.282C= ENSP00000468349.1:p.Cys94=
ENST00000588919.5:c.321C= ENSP00000464989.3:p.Cys107=
ENST00000589115.5:c.402C= ENSP00000466872.2:p.Cys134=
ENST00000592940.2:n.341C=
ENST00000593032.5:c.321C= ENSP00000465828.3:p.Cys107=
ENST00000611653.4:c.321C= ENSP00000483655.1:p.Cys107=
ENST00000616066.4:c.399C= ENSP00000485000.1:p.Cys133=
ENST00000622390.4:c.510C= ENSP00000477503.1:p.Cys170=
NM_001039847.2:c.402C= NP_001034936.1:p.Cys134=
NM_001039848.2:c.513C= NP_001034937.1:p.Cys171=
NM_002085.4:c.402C= NP_002076.2:p.Cys134=
NM_001039848.3:c.513C= NP_001034937.1:p.Cys171=
NM_001039847.3:c.402C= NP_001034936.1:p.Cys134=
NM_001039848.4:c.513C= NP_001034937.1:p.Cys171=
NM_001367832.1:c.321C= NP_001354761.1:p.Cys107=
NM_002085.5:c.402C= MANE Select NP_002076.2:p.Cys134=