Canonical Allele Identifier: CA402937597

Gene: GPX4

Linked Data

• dbSNP Id: rs1373540032
• gnomAD v2: 19-1105757-C-T
• gnomAD v3: 19-1105758-C-T
• gnomAD v4: 19-1105758-C-T
• MyVariant Identifiers: chr19:g.1105757C>T (hg19) ; chr19:g.1105758C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105758C>T , CM000681.2:g.1105758C>T	GRCh38
NC_000019.9:g.1105757C>T , CM000681.1:g.1105757C>T	GRCh37
NC_000019.8:g.1056757C>T	NCBI36
NG_050621.1:g.6833C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.536C>T	ENSP00000473614.3:p.Pro179Leu
ENST00000593032.6:c.344C>T	ENSP00000465828.4:p.Pro115Leu
ENST00000706713.1:c.419C>T	ENSP00000516510.1:p.Pro140Leu
ENST00000706714.1:c.344C>T	ENSP00000516511.1:p.Pro115Leu
ENST00000706715.1:c.41C>T	ENSP00000516512.1:p.Pro14Leu
ENST00000354171.13:c.425C>T MANE Select	ENSP00000346103.7:p.Pro142Leu
ENST00000589115.6:c.425C>T	ENSP00000466872.3:p.Pro142Leu
ENST00000354171.12:c.425C>T	ENSP00000346103.7:p.Pro142Leu
ENST00000585362.6:c.536C>T	ENSP00000473614.2:p.Pro179Leu
ENST00000585480.1:c.158C>T	ENSP00000467900.1:p.Pro53Leu
ENST00000587648.5:c.305C>T	ENSP00000468349.1:p.Pro102Leu
ENST00000588919.5:c.344C>T	ENSP00000464989.3:p.Pro115Leu
ENST00000589115.5:c.425C>T	ENSP00000466872.2:p.Pro142Leu
ENST00000592940.2:n.364C>T
ENST00000593032.5:c.344C>T	ENSP00000465828.3:p.Pro115Leu
ENST00000611653.4:c.344C>T	ENSP00000483655.1:p.Pro115Leu
ENST00000616066.4:c.422C>T	ENSP00000485000.1:p.Pro141Leu
ENST00000622390.4:c.533C>T	ENSP00000477503.1:p.Pro178Leu
NM_001039847.2:c.425C>T	NP_001034936.1:p.Pro142Leu
NM_001039848.2:c.536C>T	NP_001034937.1:p.Pro179Leu
NM_002085.4:c.425C>T	NP_002076.2:p.Pro142Leu
NM_001039848.3:c.536C>T	NP_001034937.1:p.Pro179Leu
NM_001039847.3:c.425C>T	NP_001034936.1:p.Pro142Leu
NM_001039848.4:c.536C>T	NP_001034937.1:p.Pro179Leu
NM_001367832.1:c.344C>T	NP_001354761.1:p.Pro115Leu
NM_002085.5:c.425C>T MANE Select	NP_002076.2:p.Pro142Leu