Canonical Allele Identifier: CA402934211
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104084T>G , CM000681.2:g.1104084T>G GRCh38
NC_000019.9:g.1104083T>G , CM000681.1:g.1104083T>G GRCh37
NC_000019.8:g.1055083T>G NCBI36
NG_050621.1:g.5159T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000593032.6:c.-41T>G ENSP00000465828.4:n.-41T>G
ENST00000706713.1:c.41T>G ENSP00000516510.1:p.Leu14Arg
ENST00000706714.1:c.-41T>G ENSP00000516511.1:n.-41T>G
ENST00000354171.13:c.41T>G MANE Select ENSP00000346103.7:p.Leu14Arg
ENST00000589115.6:c.41T>G ENSP00000466872.3:p.Leu14Arg
ENST00000354171.12:c.41T>G ENSP00000346103.7:p.Leu14Arg
ENST00000588919.5:c.-41T>G ENSP00000464989.3:n.-41T>G
ENST00000589115.5:c.41T>G ENSP00000466872.2:p.Leu14Arg
ENST00000593032.5:c.-41T>G ENSP00000465828.3:n.-41T>G
ENST00000611653.4:c.-41T>G ENSP00000483655.1:n.-41T>G
ENST00000616066.4:c.41T>G ENSP00000485000.1:p.Leu14Arg
NM_001039847.2:c.41T>G NP_001034936.1:p.Leu14Arg
NM_002085.4:c.41T>G NP_002076.2:p.Leu14Arg
NM_001039847.3:c.41T>G NP_001034936.1:p.Leu14Arg
NM_001367832.1:c.-41T>G NP_001354761.1:n.-41T>G
NM_002085.5:c.41T>G MANE Select NP_002076.2:p.Leu14Arg