Canonical Allele Identifier: CA303992496
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1046435919
gnomAD v2: 19-1104048-C-T
gnomAD v3: 19-1104049-C-T
gnomAD v4: 19-1104049-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104049C>T , CM000681.2:g.1104049C>T GRCh38
NC_000019.9:g.1104048C>T , CM000681.1:g.1104048C>T GRCh37
NC_000019.8:g.1055048C>T NCBI36
NG_050621.1:g.5124C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.6C>T ENSP00000516510.1:p.Ser2=
ENST00000354171.13:c.6C>T MANE Select ENSP00000346103.7:p.Ser2=
ENST00000589115.6:c.6C>T ENSP00000466872.3:p.Ser2=
ENST00000354171.12:c.6C>T ENSP00000346103.7:p.Ser2=
ENST00000589115.5:c.6C>T ENSP00000466872.2:p.Ser2=
ENST00000616066.4:c.6C>T ENSP00000485000.1:p.Ser2=
NM_001039847.2:c.6C>T NP_001034936.1:p.Ser2=
NM_002085.4:c.6C>T NP_002076.2:p.Ser2=
NM_001039847.3:c.6C>T NP_001034936.1:p.Ser2=
NM_002085.5:c.6C>T MANE Select NP_002076.2:p.Ser2=