Canonical Allele Identifier: CA2588205800

Gene: GPX4

Linked Data

• gnomAD v4: 19-1104020-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104020C>G , CM000681.2:g.1104020C>G	GRCh38
NC_000019.9:g.1104019C>G , CM000681.1:g.1104019C>G	GRCh37
NC_000019.8:g.1055019C>G	NCBI36
NG_050621.1:g.5095C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706713.1:c.-24C>G	ENSP00000516510.1:n.-24C>G
ENST00000354171.13:c.-24C>G MANE Select	ENSP00000346103.7:n.-24C>G
ENST00000589115.6:c.-24C>G	ENSP00000466872.3:n.-24C>G
ENST00000354171.12:c.-24C>G	ENSP00000346103.7:n.-24C>G
ENST00000589115.5:c.-24C>G	ENSP00000466872.2:n.-24C>G
ENST00000616066.4:c.-24C>G	ENSP00000485000.1:n.-24C>G
NM_001039847.2:c.-24C>G	NP_001034936.1:n.-24C>G
NM_002085.4:c.-24C>G	NP_002076.2:n.-24C>G
NM_001039847.3:c.-24C>G	NP_001034936.1:n.-24C>G
NM_002085.5:c.-24C>G MANE Select	NP_002076.2:n.-24C>G