Canonical Allele Identifier: CA9037486

Gene: GPX4

Linked Data

• ClinVar Variation Id: 2142226
• ClinVar RCV Id: RCV003058955
• dbSNP Id: rs781320737
• ExAC: 19:1106462 G / T
• gnomAD v2: 19-1106462-G-T
• gnomAD v3: 19-1106463-G-T
• gnomAD v4: 19-1106463-G-T
• MyVariant Identifiers: chr19:g.1106462G>T (hg19) ; chr19:g.1106463G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106463G>T , CM000681.2:g.1106463G>T	GRCh38
NC_000019.9:g.1106462G>T , CM000681.1:g.1106462G>T	GRCh37
NC_000019.8:g.1057462G>T	NCBI36
NG_050621.1:g.7538G>T

Transcript Alleles

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