Canonical Allele Identifier: CA9037491

Gene: GPX4

Linked Data

• ClinVar Variation Id: 1988693
• ClinVar RCV Id: RCV002781428
• dbSNP Id: rs373571319
• ExAC: 19:1106471 T / C
• gnomAD v2: 19-1106471-T-C
• gnomAD v3: 19-1106472-T-C
• gnomAD v4: 19-1106472-T-C
• MyVariant Identifiers: chr19:g.1106471T>C (hg19) ; chr19:g.1106472T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106472T>C , CM000681.2:g.1106472T>C	GRCh38
NC_000019.9:g.1106471T>C , CM000681.1:g.1106471T>C	GRCh37
NC_000019.8:g.1057471T>C	NCBI36
NG_050621.1:g.7547T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.672+13T>C	ENSP00000473614.3:n.672+13T>C
ENST00000593032.6:c.541+13T>C	ENSP00000465828.4:n.541+13T>C
ENST00000706713.1:c.555+13T>C	ENSP00000516510.1:n.555+13T>C
ENST00000706714.1:c.541+13T>C	ENSP00000516511.1:n.541+13T>C
ENST00000706715.1:c.177+13T>C	ENSP00000516512.1:n.177+13T>C
ENST00000354171.13:c.561+13T>C MANE Select	ENSP00000346103.7:n.561+13T>C
ENST00000589115.6:c.536+13T>C	ENSP00000466872.3:n.536+13T>C
ENST00000354171.12:c.561+13T>C	ENSP00000346103.7:n.561+13T>C
ENST00000585480.1:c.294+13T>C	ENSP00000467900.1:n.294+13T>C
ENST00000587648.5:c.441+13T>C	ENSP00000468349.1:n.441+13T>C
ENST00000588919.5:c.502+13T>C	ENSP00000464989.3:n.502+13T>C
ENST00000589115.5:c.536+13T>C	ENSP00000466872.2:n.536+13T>C
ENST00000592940.2:n.932+13T>C
ENST00000611653.4:c.480+13T>C	ENSP00000483655.1:n.480+13T>C
ENST00000616066.4:c.558+13T>C	ENSP00000485000.1:n.558+13T>C
ENST00000622390.4:c.669+13T>C	ENSP00000477503.1:n.669+13T>C
NM_001039847.2:c.583+13T>C	NP_001034936.1:n.583+13T>C
NM_001039848.2:c.672+13T>C	NP_001034937.1:n.672+13T>C
NM_002085.4:c.561+13T>C	NP_002076.2:n.561+13T>C
NM_001039848.3:c.672+13T>C	NP_001034937.1:n.672+13T>C
NM_001039847.3:c.583+13T>C	NP_001034936.1:n.583+13T>C
NM_001039848.4:c.672+13T>C	NP_001034937.1:n.672+13T>C
NM_001367832.1:c.480+13T>C	NP_001354761.1:n.480+13T>C
NM_002085.5:c.561+13T>C MANE Select	NP_002076.2:n.561+13T>C