Canonical Allele Identifier: CA2588207962

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106781-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106781C>G , CM000681.2:g.1106781C>G	GRCh38
NC_000019.9:g.1106780C>G , CM000681.1:g.1106780C>G	GRCh37
NC_000019.8:g.1057780C>G	NCBI36
NG_050621.1:g.7856C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354171.12:c.*209C>G	ENSP00000346103.7:n.*209C>G
ENST00000588919.5:c.*15C>G	ENSP00000464989.3:n.*15C>G
ENST00000592940.2:n.1174C>G
ENST00000616066.4:c.*209C>G	ENSP00000485000.1:n.*209C>G
ENST00000622390.4:c.*209C>G	ENSP00000477503.1:n.*209C>G
NM_001039847.2:c.*141C>G	NP_001034936.1:n.*141C>G
NM_001039848.2:c.*209C>G	NP_001034937.1:n.*209C>G
NM_002085.4:c.*209C>G	NP_002076.2:n.*209C>G
NM_001039848.3:c.*209C>G	NP_001034937.1:n.*209C>G