Canonical Allele Identifier: CA2317519065
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104092G= , CM000681.2:g.1104092G= GRCh38
NC_000019.9:g.1104091G= , CM000681.1:g.1104091G= GRCh37
NC_000019.8:g.1055091G= NCBI36
NG_050621.1:g.5167G=

Transcript Alleles

HGVS Amino-acid change
ENST00000593032.6:c.-33G= ENSP00000465828.4:n.-33G=
ENST00000706713.1:c.49G= ENSP00000516510.1:p.Gly17=
ENST00000706714.1:c.-33G= ENSP00000516511.1:n.-33G=
ENST00000354171.13:c.49G= MANE Select ENSP00000346103.7:p.Gly17=
ENST00000589115.6:c.49G= ENSP00000466872.3:p.Gly17=
ENST00000354171.12:c.49G= ENSP00000346103.7:p.Gly17=
ENST00000588919.5:c.-33G= ENSP00000464989.3:n.-33G=
ENST00000589115.5:c.49G= ENSP00000466872.2:p.Gly17=
ENST00000593032.5:c.-33G= ENSP00000465828.3:n.-33G=
ENST00000611653.4:c.-33G= ENSP00000483655.1:n.-33G=
ENST00000616066.4:c.49G= ENSP00000485000.1:p.Gly17=
NM_001039847.2:c.49G= NP_001034936.1:p.Gly17=
NM_002085.4:c.49G= NP_002076.2:p.Gly17=
NM_001039847.3:c.49G= NP_001034936.1:p.Gly17=
NM_001367832.1:c.-33G= NP_001354761.1:n.-33G=
NM_002085.5:c.49G= MANE Select NP_002076.2:p.Gly17=