Canonical Allele Identifier: CA2588205807
Gene: GPX4 HGNC NCBI

Linked Data

gnomAD v4: 19-1104024-T-TGGCTCCCAGCCCCGCC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104026_1104041dup , CM000681.2:g.1104026_1104041dup GRCh38
NC_000019.9:g.1104025_1104040dup , CM000681.1:g.1104025_1104040dup GRCh37
NC_000019.8:g.1055025_1055040dup NCBI36
NG_050621.1:g.5101_5116dup

Transcript Alleles

HGVS Amino-acid change
ENST00000706713.1:c.-18_-3dup ENSP00000516510.1:n.-18_-3dup
ENST00000354171.13:c.-18_-3dup MANE Select ENSP00000346103.7:n.-18_-3dup
ENST00000589115.6:c.-18_-3dup ENSP00000466872.3:n.-18_-3dup
ENST00000354171.12:c.-18_-3dup ENSP00000346103.7:n.-18_-3dup
ENST00000589115.5:c.-18_-3dup ENSP00000466872.2:n.-18_-3dup
ENST00000616066.4:c.-18_-3dup ENSP00000485000.1:n.-18_-3dup
NM_001039847.2:c.-18_-3dup NP_001034936.1:n.-18_-3dup
NM_002085.4:c.-18_-3dup NP_002076.2:n.-18_-3dup
NM_001039847.3:c.-18_-3dup NP_001034936.1:n.-18_-3dup
NM_002085.5:c.-18_-3dup MANE Select NP_002076.2:n.-18_-3dup
Search 100 bp 5'
Search 100 bp 3'