Canonical Allele Identifier: CA303992459
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs976848690
gnomAD v4: 19-1104015-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104015A>G , CM000681.2:g.1104015A>G GRCh38
NC_000019.9:g.1104014A>G , CM000681.1:g.1104014A>G GRCh37
NC_000019.8:g.1055014A>G NCBI36
NG_050621.1:g.5090A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-29A>G ENSP00000516510.1:n.-29A>G
ENST00000354171.13:c.-29A>G MANE Select ENSP00000346103.7:n.-29A>G
ENST00000589115.6:c.-29A>G ENSP00000466872.3:n.-29A>G
ENST00000354171.12:c.-29A>G ENSP00000346103.7:n.-29A>G
ENST00000589115.5:c.-29A>G ENSP00000466872.2:n.-29A>G
ENST00000616066.4:c.-29A>G ENSP00000485000.1:n.-29A>G
NM_001039847.2:c.-29A>G NP_001034936.1:n.-29A>G
NM_002085.4:c.-29A>G NP_002076.2:n.-29A>G
NM_001039847.3:c.-29A>G NP_001034936.1:n.-29A>G
NM_002085.5:c.-29A>G MANE Select NP_002076.2:n.-29A>G