Canonical Allele Identifier: CA402939276

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106266-G-A
• MyVariant Identifiers: chr19:g.1106265G>A (hg19) ; chr19:g.1106266G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106266G>A , CM000681.2:g.1106266G>A	GRCh38
NC_000019.9:g.1106265G>A , CM000681.1:g.1106265G>A	GRCh37
NC_000019.8:g.1057265G>A	NCBI36
NG_050621.1:g.7341G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.612G>A	ENSP00000473614.3:p.Lys204=
ENST00000593032.6:c.481G>A	ENSP00000465828.4:p.Val161Ile
ENST00000706713.1:c.495G>A	ENSP00000516510.1:p.Lys165=
ENST00000706714.1:c.481G>A	ENSP00000516511.1:p.Val161Ile
ENST00000706715.1:c.117G>A	ENSP00000516512.1:p.Lys39=
ENST00000354171.13:c.501G>A MANE Select	ENSP00000346103.7:p.Lys167=
ENST00000589115.6:c.477-134G>A	ENSP00000466872.3:n.477-134G>A
ENST00000354171.12:c.501G>A	ENSP00000346103.7:p.Lys167=
ENST00000585480.1:c.234G>A	ENSP00000467900.1:p.Lys78=
ENST00000587648.5:c.381G>A	ENSP00000468349.1:p.Lys127=
ENST00000588919.5:c.420G>A	ENSP00000464989.3:p.Lys140=
ENST00000589115.5:c.477-134G>A	ENSP00000466872.2:n.477-134G>A
ENST00000592940.2:n.872G>A
ENST00000593032.5:c.481G>A	ENSP00000465828.3:p.Val161Ile
ENST00000611653.4:c.420G>A	ENSP00000483655.1:p.Lys140=
ENST00000616066.4:c.498G>A	ENSP00000485000.1:p.Lys166=
ENST00000622390.4:c.609G>A	ENSP00000477503.1:p.Lys203=
NM_001039847.2:c.501G>A	NP_001034936.1:p.Lys167=
NM_001039848.2:c.612G>A	NP_001034937.1:p.Lys204=
NM_002085.4:c.501G>A	NP_002076.2:p.Lys167=
NM_001039848.3:c.612G>A	NP_001034937.1:p.Lys204=
NM_001039847.3:c.501G>A	NP_001034936.1:p.Lys167=
NM_001039848.4:c.612G>A	NP_001034937.1:p.Lys204=
NM_001367832.1:c.420G>A	NP_001354761.1:p.Lys140=
NM_002085.5:c.501G>A MANE Select	NP_002076.2:p.Lys167=