Canonical Allele Identifier: CA2588205806
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1104024-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104024T>G , CM000681.2:g.1104024T>G GRCh38
NC_000019.9:g.1104023T>G , CM000681.1:g.1104023T>G GRCh37
NC_000019.8:g.1055023T>G NCBI36
NG_050621.1:g.5099T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-20T>G ENSP00000516510.1:n.-20T>G
ENST00000354171.13:c.-20T>G MANE Select ENSP00000346103.7:n.-20T>G
ENST00000589115.6:c.-20T>G ENSP00000466872.3:n.-20T>G
ENST00000354171.12:c.-20T>G ENSP00000346103.7:n.-20T>G
ENST00000589115.5:c.-20T>G ENSP00000466872.2:n.-20T>G
ENST00000616066.4:c.-20T>G ENSP00000485000.1:n.-20T>G
NM_001039847.2:c.-20T>G NP_001034936.1:n.-20T>G
NM_002085.4:c.-20T>G NP_002076.2:n.-20T>G
NM_001039847.3:c.-20T>G NP_001034936.1:n.-20T>G
NM_002085.5:c.-20T>G MANE Select NP_002076.2:n.-20T>G