Canonical Allele Identifier: CA2317520886

Gene: GPX4

Linked Data

• dbSNP Id: rs2079664939

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106779G>A , CM000681.2:g.1106779G>A	GRCh38
NC_000019.9:g.1106778G>A , CM000681.1:g.1106778G>A	GRCh37
NC_000019.8:g.1057778G>A	NCBI36
NG_050621.1:g.7854G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*207G>A	ENSP00000473614.3:n.*207G>A
ENST00000706713.1:c.*207G>A	ENSP00000516510.1:n.*207G>A
ENST00000354171.13:c.*207G>A MANE Select	ENSP00000346103.7:n.*207G>A
ENST00000589115.6:c.*233G>A	ENSP00000466872.3:n.*233G>A
ENST00000354171.12:c.*207G>A	ENSP00000346103.7:n.*207G>A
ENST00000585480.1:c.501G>A	ENSP00000467900.1:p.Ter167=
ENST00000588919.5:c.*13G>A	ENSP00000464989.3:n.*13G>A
ENST00000589115.5:c.*233G>A	ENSP00000466872.2:n.*233G>A
ENST00000592940.2:n.1172G>A
ENST00000611653.4:c.*207G>A	ENSP00000483655.1:n.*207G>A
ENST00000616066.4:c.*207G>A	ENSP00000485000.1:n.*207G>A
ENST00000622390.4:c.*207G>A	ENSP00000477503.1:n.*207G>A
NM_001039847.2:c.*139G>A	NP_001034936.1:n.*139G>A
NM_001039848.2:c.*207G>A	NP_001034937.1:n.*207G>A
NM_002085.4:c.*207G>A	NP_002076.2:n.*207G>A
NM_001039848.3:c.*207G>A	NP_001034937.1:n.*207G>A
NM_001039847.3:c.*139G>A	NP_001034936.1:n.*139G>A
NM_001039848.4:c.*207G>A	NP_001034937.1:n.*207G>A
NM_001367832.1:c.*207G>A	NP_001354761.1:n.*207G>A
NM_002085.5:c.*207G>A MANE Select	NP_002076.2:n.*207G>A