Canonical Allele Identifier: CA9037133
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs767130132
gnomAD v2: 19-1104106-C-G
gnomAD v3: 19-1104107-C-G
gnomAD v4: 19-1104107-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104107C>G , CM000681.2:g.1104107C>G GRCh38
NC_000019.9:g.1104106C>G , CM000681.1:g.1104106C>G GRCh37
NC_000019.8:g.1055106C>G NCBI36
NG_050621.1:g.5182C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593032.6:c.-18C>G ENSP00000465828.4:n.-18C>G
ENST00000706713.1:c.64C>G ENSP00000516510.1:p.Pro22Ala
ENST00000706714.1:c.-18C>G ENSP00000516511.1:n.-18C>G
ENST00000354171.13:c.64C>G MANE Select ENSP00000346103.7:p.Pro22Ala
ENST00000589115.6:c.64C>G ENSP00000466872.3:p.Pro22Ala
ENST00000354171.12:c.64C>G ENSP00000346103.7:p.Pro22Ala
ENST00000588919.5:c.-18C>G ENSP00000464989.3:n.-18C>G
ENST00000589115.5:c.64C>G ENSP00000466872.2:p.Pro22Ala
ENST00000593032.5:c.-18C>G ENSP00000465828.3:n.-18C>G
ENST00000611653.4:c.-18C>G ENSP00000483655.1:n.-18C>G
ENST00000616066.4:c.64C>G ENSP00000485000.1:p.Pro22Ala
NM_001039847.2:c.64C>G NP_001034936.1:p.Pro22Ala
NM_002085.4:c.64C>G NP_002076.2:p.Pro22Ala
NM_001039847.3:c.64C>G NP_001034936.1:p.Pro22Ala
NM_001367832.1:c.-18C>G NP_001354761.1:n.-18C>G
NM_002085.5:c.64C>G MANE Select NP_002076.2:p.Pro22Ala