Canonical Allele Identifier: CA2838366294

Gene: GPX4

Genomic Alleles

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

Transcript Alleles

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