Canonical Allele Identifier: CA2588205782
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1104007-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104007A>T , CM000681.2:g.1104007A>T GRCh38
NC_000019.9:g.1104006A>T , CM000681.1:g.1104006A>T GRCh37
NC_000019.8:g.1055006A>T NCBI36
NG_050621.1:g.5082A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-37A>T ENSP00000516510.1:n.-37A>T
ENST00000354171.13:c.-37A>T MANE Select ENSP00000346103.7:n.-37A>T
ENST00000354171.12:c.-37A>T ENSP00000346103.7:n.-37A>T
ENST00000616066.4:c.-37A>T ENSP00000485000.1:n.-37A>T
NM_001039847.2:c.-37A>T NP_001034936.1:n.-37A>T
NM_002085.4:c.-37A>T NP_002076.2:n.-37A>T
NM_001039847.3:c.-37A>T NP_001034936.1:n.-37A>T
NM_002085.5:c.-37A>T MANE Select NP_002076.2:n.-37A>T