Canonical Allele Identifier: CA9037522

Gene: GPX4

Linked Data

• dbSNP Id: rs752733635
• ExAC: 19:1106541 G / T
• gnomAD v2: 19-1106541-G-T
• gnomAD v4: 19-1106542-G-T
• MyVariant Identifiers: chr19:g.1106541G>T (hg19) ; chr19:g.1106542G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106542G>T , CM000681.2:g.1106542G>T	GRCh38
NC_000019.9:g.1106541G>T , CM000681.1:g.1106541G>T	GRCh37
NC_000019.8:g.1057541G>T	NCBI36
NG_050621.1:g.7617G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.675G>T	ENSP00000473614.3:p.Val225=
ENST00000593032.6:c.544G>T	ENSP00000465828.4:p.Asp182Tyr
ENST00000706713.1:c.558G>T	ENSP00000516510.1:p.Val186=
ENST00000706714.1:c.544G>T	ENSP00000516511.1:p.Asp182Tyr
ENST00000706715.1:c.180G>T	ENSP00000516512.1:p.Val60=
ENST00000354171.13:c.564G>T MANE Select	ENSP00000346103.7:p.Val188=
ENST00000589115.6:c.539G>T	ENSP00000466872.3:p.Ter180Leu
ENST00000354171.12:c.564G>T	ENSP00000346103.7:p.Val188=
ENST00000585480.1:c.295-31G>T	ENSP00000467900.1:n.295-31G>T
ENST00000587648.5:c.444G>T	ENSP00000468349.1:p.Val148=
ENST00000588919.5:c.505G>T	ENSP00000464989.3:p.Asp169Tyr
ENST00000589115.5:c.539G>T	ENSP00000466872.2:p.Ter180Leu
ENST00000592940.2:n.935G>T
ENST00000611653.4:c.483G>T	ENSP00000483655.1:p.Val161=
ENST00000616066.4:c.561G>T	ENSP00000485000.1:p.Val187=
ENST00000622390.4:c.672G>T	ENSP00000477503.1:p.Val224=
NM_001039847.2:c.586G>T	NP_001034936.1:p.Asp196Tyr
NM_001039848.2:c.675G>T	NP_001034937.1:p.Val225=
NM_002085.4:c.564G>T	NP_002076.2:p.Val188=
NM_001039848.3:c.675G>T	NP_001034937.1:p.Val225=
NM_001039847.3:c.586G>T	NP_001034936.1:p.Asp196Tyr
NM_001039848.4:c.675G>T	NP_001034937.1:p.Val225=
NM_001367832.1:c.483G>T	NP_001354761.1:p.Val161=
NM_002085.5:c.564G>T MANE Select	NP_002076.2:p.Val188=