Canonical Allele Identifier: CA9037345

Gene: GPX4

Linked Data

• ClinVar Variation Id: 1666222
• ClinVar RCV Id: RCV002186211
• dbSNP Id: rs747423599
• ExAC: 19:1105731 C / T
• gnomAD v2: 19-1105731-C-T
• gnomAD v4: 19-1105732-C-T
• MyVariant Identifiers: chr19:g.1105731C>T (hg19) ; chr19:g.1105732C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105732C>T , CM000681.2:g.1105732C>T	GRCh38
NC_000019.9:g.1105731C>T , CM000681.1:g.1105731C>T	GRCh37
NC_000019.8:g.1056731C>T	NCBI36
NG_050621.1:g.6807C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.510C>T	ENSP00000473614.3:p.Ile170=
ENST00000593032.6:c.318C>T	ENSP00000465828.4:p.Ile106=
ENST00000706713.1:c.393C>T	ENSP00000516510.1:p.Ile131=
ENST00000706714.1:c.318C>T	ENSP00000516511.1:p.Ile106=
ENST00000706715.1:c.15C>T	ENSP00000516512.1:p.Ile5=
ENST00000354171.13:c.399C>T MANE Select	ENSP00000346103.7:p.Ile133=
ENST00000589115.6:c.399C>T	ENSP00000466872.3:p.Ile133=
ENST00000354171.12:c.399C>T	ENSP00000346103.7:p.Ile133=
ENST00000585362.6:c.510C>T	ENSP00000473614.2:p.Ile170=
ENST00000585480.1:c.132C>T	ENSP00000467900.1:p.Ile44=
ENST00000587648.5:c.279C>T	ENSP00000468349.1:p.Ile93=
ENST00000588919.5:c.318C>T	ENSP00000464989.3:p.Ile106=
ENST00000589115.5:c.399C>T	ENSP00000466872.2:p.Ile133=
ENST00000592940.2:n.338C>T
ENST00000593032.5:c.318C>T	ENSP00000465828.3:p.Ile106=
ENST00000611653.4:c.318C>T	ENSP00000483655.1:p.Ile106=
ENST00000616066.4:c.396C>T	ENSP00000485000.1:p.Ile132=
ENST00000622390.4:c.507C>T	ENSP00000477503.1:p.Ile169=
NM_001039847.2:c.399C>T	NP_001034936.1:p.Ile133=
NM_001039848.2:c.510C>T	NP_001034937.1:p.Ile170=
NM_002085.4:c.399C>T	NP_002076.2:p.Ile133=
NM_001039848.3:c.510C>T	NP_001034937.1:p.Ile170=
NM_001039847.3:c.399C>T	NP_001034936.1:p.Ile133=
NM_001039848.4:c.510C>T	NP_001034937.1:p.Ile170=
NM_001367832.1:c.318C>T	NP_001354761.1:p.Ile106=
NM_002085.5:c.399C>T MANE Select	NP_002076.2:p.Ile133=