Canonical Allele Identifier: CA2317520893
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs1015811628
gnomAD v4: 19-1106787-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106787G>C , CM000681.2:g.1106787G>C GRCh38
NC_000019.9:g.1106786G>C , CM000681.1:g.1106786G>C GRCh37
NC_000019.8:g.1057786G>C NCBI36
NG_050621.1:g.7862G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000354171.12:c.*215G>C ENSP00000346103.7:n.*215G>C
ENST00000588919.5:c.*21G>C ENSP00000464989.3:n.*21G>C
ENST00000592940.2:n.1180G>C
ENST00000616066.4:c.*215G>C ENSP00000485000.1:n.*215G>C
ENST00000622390.4:c.*215G>C ENSP00000477503.1:n.*215G>C
NM_001039847.2:c.*147G>C NP_001034936.1:n.*147G>C
NM_001039848.2:c.*215G>C NP_001034937.1:n.*215G>C
NM_002085.4:c.*215G>C NP_002076.2:n.*215G>C
NM_001039848.3:c.*215G>C NP_001034937.1:n.*215G>C
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