Canonical Allele Identifier: CA9037555

Gene: GPX4

Linked Data

• dbSNP Id: rs556962104
• ExAC: 19:1106616 G / C
• gnomAD v2: 19-1106616-G-C
• gnomAD v3: 19-1106617-G-C
• gnomAD v4: 19-1106617-G-C
• MyVariant Identifiers: chr19:g.1106616G>C (hg19) ; chr19:g.1106617G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106617G>C , CM000681.2:g.1106617G>C	GRCh38
NC_000019.9:g.1106616G>C , CM000681.1:g.1106616G>C	GRCh37
NC_000019.8:g.1057616G>C	NCBI36
NG_050621.1:g.7692G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.*45G>C	ENSP00000473614.3:n.*45G>C
ENST00000593032.6:c.619G>C	ENSP00000465828.4:p.Gly207Arg
ENST00000706713.1:c.*45G>C	ENSP00000516510.1:n.*45G>C
ENST00000706714.1:c.619G>C	ENSP00000516511.1:p.Gly207Arg
ENST00000706715.1:c.*45G>C	ENSP00000516512.1:n.*45G>C
ENST00000354171.13:c.*45G>C MANE Select	ENSP00000346103.7:n.*45G>C
ENST00000589115.6:c.*71G>C	ENSP00000466872.3:n.*71G>C
ENST00000354171.12:c.*45G>C	ENSP00000346103.7:n.*45G>C
ENST00000585480.1:c.339G>C	ENSP00000467900.1:p.Leu113Phe
ENST00000588919.5:c.580G>C	ENSP00000464989.3:p.Gly194Arg
ENST00000589115.5:c.*71G>C	ENSP00000466872.2:n.*71G>C
ENST00000592940.2:n.1010G>C
ENST00000611653.4:c.*45G>C	ENSP00000483655.1:n.*45G>C
ENST00000616066.4:c.*45G>C	ENSP00000485000.1:n.*45G>C
ENST00000622390.4:c.*45G>C	ENSP00000477503.1:n.*45G>C
NM_001039847.2:c.661G>C	NP_001034936.1:p.Gly221Arg
NM_001039848.2:c.*45G>C	NP_001034937.1:n.*45G>C
NM_002085.4:c.*45G>C	NP_002076.2:n.*45G>C
NM_001039848.3:c.*45G>C	NP_001034937.1:n.*45G>C
NM_001039847.3:c.661G>C	NP_001034936.1:p.Gly221Arg
NM_001039848.4:c.*45G>C	NP_001034937.1:n.*45G>C
NM_001367832.1:c.*45G>C	NP_001354761.1:n.*45G>C
NM_002085.5:c.*45G>C MANE Select	NP_002076.2:n.*45G>C