Canonical Allele Identifier: CA992487278

Gene: GPX4

Linked Data

• dbSNP Id: rs2079618982
• gnomAD v4: 19-1104019-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104019G>C , CM000681.2:g.1104019G>C	GRCh38
NC_000019.9:g.1104018G>C , CM000681.1:g.1104018G>C	GRCh37
NC_000019.8:g.1055018G>C	NCBI36
NG_050621.1:g.5094G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706713.1:c.-25G>C	ENSP00000516510.1:n.-25G>C
ENST00000354171.13:c.-25G>C MANE Select	ENSP00000346103.7:n.-25G>C
ENST00000589115.6:c.-25G>C	ENSP00000466872.3:n.-25G>C
ENST00000354171.12:c.-25G>C	ENSP00000346103.7:n.-25G>C
ENST00000589115.5:c.-25G>C	ENSP00000466872.2:n.-25G>C
ENST00000616066.4:c.-25G>C	ENSP00000485000.1:n.-25G>C
NM_001039847.2:c.-25G>C	NP_001034936.1:n.-25G>C
NM_002085.4:c.-25G>C	NP_002076.2:n.-25G>C
NM_001039847.3:c.-25G>C	NP_001034936.1:n.-25G>C
NM_002085.5:c.-25G>C MANE Select	NP_002076.2:n.-25G>C