Canonical Allele Identifier: CA303994989

Gene: GPX4

Linked Data

• dbSNP Id: rs997019810
• gnomAD v3: 19-1106459-G-A
• gnomAD v4: 19-1106459-G-A
• MyVariant Identifiers: chr19:g.1106458G>A (hg19) ; chr19:g.1106459G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106459G>A , CM000681.2:g.1106459G>A	GRCh38
NC_000019.9:g.1106458G>A , CM000681.1:g.1106458G>A	GRCh37
NC_000019.8:g.1057458G>A	NCBI36
NG_050621.1:g.7534G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.672G>A	ENSP00000473614.3:p.Leu224=
ENST00000593032.6:c.541G>A	ENSP00000465828.4:p.Gly181Ser
ENST00000706713.1:c.555G>A	ENSP00000516510.1:p.Leu185=
ENST00000706714.1:c.541G>A	ENSP00000516511.1:p.Gly181Ser
ENST00000706715.1:c.177G>A	ENSP00000516512.1:p.Leu59=
ENST00000354171.13:c.561G>A MANE Select	ENSP00000346103.7:p.Leu187=
ENST00000589115.6:c.536G>A	ENSP00000466872.3:p.Trp179Ter
ENST00000354171.12:c.561G>A	ENSP00000346103.7:p.Leu187=
ENST00000585480.1:c.294G>A	ENSP00000467900.1:p.Leu98=
ENST00000587648.5:c.441G>A	ENSP00000468349.1:p.Leu147=
ENST00000588919.5:c.502G>A	ENSP00000464989.3:p.Gly168Ser
ENST00000589115.5:c.536G>A	ENSP00000466872.2:p.Trp179Ter
ENST00000592940.2:n.932G>A
ENST00000611653.4:c.480G>A	ENSP00000483655.1:p.Leu160=
ENST00000616066.4:c.558G>A	ENSP00000485000.1:p.Leu186=
ENST00000622390.4:c.669G>A	ENSP00000477503.1:p.Leu223=
NM_001039847.2:c.583G>A	NP_001034936.1:p.Gly195Ser
NM_001039848.2:c.672G>A	NP_001034937.1:p.Leu224=
NM_002085.4:c.561G>A	NP_002076.2:p.Leu187=
NM_001039848.3:c.672G>A	NP_001034937.1:p.Leu224=
NM_001039847.3:c.583G>A	NP_001034936.1:p.Gly195Ser
NM_001039848.4:c.672G>A	NP_001034937.1:p.Leu224=
NM_001367832.1:c.480G>A	NP_001354761.1:p.Leu160=
NM_002085.5:c.561G>A MANE Select	NP_002076.2:p.Leu187=