Canonical Allele Identifier: CA303992464
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1023943971

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104025G>A , CM000681.2:g.1104025G>A GRCh38
NC_000019.9:g.1104024G>A , CM000681.1:g.1104024G>A GRCh37
NC_000019.8:g.1055024G>A NCBI36
NG_050621.1:g.5100G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-19G>A ENSP00000516510.1:n.-19G>A
ENST00000354171.13:c.-19G>A MANE Select ENSP00000346103.7:n.-19G>A
ENST00000589115.6:c.-19G>A ENSP00000466872.3:n.-19G>A
ENST00000354171.12:c.-19G>A ENSP00000346103.7:n.-19G>A
ENST00000589115.5:c.-19G>A ENSP00000466872.2:n.-19G>A
ENST00000616066.4:c.-19G>A ENSP00000485000.1:n.-19G>A
NM_001039847.2:c.-19G>A NP_001034936.1:n.-19G>A
NM_002085.4:c.-19G>A NP_002076.2:n.-19G>A
NM_001039847.3:c.-19G>A NP_001034936.1:n.-19G>A
NM_002085.5:c.-19G>A MANE Select NP_002076.2:n.-19G>A