Canonical Allele Identifier: CA2588207304

Gene: GPX4

Linked Data

• gnomAD v4: 19-1105888-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105888A>C , CM000681.2:g.1105888A>C	GRCh38
NC_000019.9:g.1105887A>C , CM000681.1:g.1105887A>C	GRCh37
NC_000019.8:g.1056887A>C	NCBI36
NG_050621.1:g.6963A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.587+79A>C	ENSP00000473614.3:n.587+79A>C
ENST00000593032.6:c.395+79A>C	ENSP00000465828.4:n.395+79A>C
ENST00000706713.1:c.470+79A>C	ENSP00000516510.1:n.470+79A>C
ENST00000706714.1:c.395+79A>C	ENSP00000516511.1:n.395+79A>C
ENST00000706715.1:c.92+79A>C	ENSP00000516512.1:n.92+79A>C
ENST00000354171.13:c.476+79A>C MANE Select	ENSP00000346103.7:n.476+79A>C
ENST00000589115.6:c.476+79A>C	ENSP00000466872.3:n.476+79A>C
ENST00000354171.12:c.476+79A>C	ENSP00000346103.7:n.476+79A>C
ENST00000585480.1:c.209+79A>C	ENSP00000467900.1:n.209+79A>C
ENST00000587648.5:c.356+79A>C	ENSP00000468349.1:n.356+79A>C
ENST00000588919.5:c.395+79A>C	ENSP00000464989.3:n.395+79A>C
ENST00000589115.5:c.476+79A>C	ENSP00000466872.2:n.476+79A>C
ENST00000592940.2:n.494A>C
ENST00000593032.5:c.395+79A>C	ENSP00000465828.3:n.395+79A>C
ENST00000611653.4:c.395+79A>C	ENSP00000483655.1:n.395+79A>C
ENST00000616066.4:c.473+79A>C	ENSP00000485000.1:n.473+79A>C
ENST00000622390.4:c.584+79A>C	ENSP00000477503.1:n.584+79A>C
NM_001039847.2:c.476+79A>C	NP_001034936.1:n.476+79A>C
NM_001039848.2:c.587+79A>C	NP_001034937.1:n.587+79A>C
NM_002085.4:c.476+79A>C	NP_002076.2:n.476+79A>C
NM_001039848.3:c.587+79A>C	NP_001034937.1:n.587+79A>C
NM_001039847.3:c.476+79A>C	NP_001034936.1:n.476+79A>C
NM_001039848.4:c.587+79A>C	NP_001034937.1:n.587+79A>C
NM_001367832.1:c.395+79A>C	NP_001354761.1:n.395+79A>C
NM_002085.5:c.476+79A>C MANE Select	NP_002076.2:n.476+79A>C