Canonical Allele Identifier: CA2588205832
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1104043-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104043G>T , CM000681.2:g.1104043G>T GRCh38
NC_000019.9:g.1104042G>T , CM000681.1:g.1104042G>T GRCh37
NC_000019.8:g.1055042G>T NCBI36
NG_050621.1:g.5118G>T

Transcript Alleles

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