Canonical Allele Identifier: CA504694667

Gene: GPX4

Linked Data

• dbSNP Id: rs1345646913
• gnomAD v2: 19-1105785-C-T
• gnomAD v4: 19-1105786-C-T
• MyVariant Identifiers: chr19:g.1105785C>T (hg19) ; chr19:g.1105786C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105786C>T , CM000681.2:g.1105786C>T	GRCh38
NC_000019.9:g.1105785C>T , CM000681.1:g.1105785C>T	GRCh37
NC_000019.8:g.1056785C>T	NCBI36
NG_050621.1:g.6861C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.564C>T	ENSP00000473614.3:p.Pro188=
ENST00000593032.6:c.372C>T	ENSP00000465828.4:p.Pro124=
ENST00000706713.1:c.447C>T	ENSP00000516510.1:p.Pro149=
ENST00000706714.1:c.372C>T	ENSP00000516511.1:p.Pro124=
ENST00000706715.1:c.69C>T	ENSP00000516512.1:p.Pro23=
ENST00000354171.13:c.453C>T MANE Select	ENSP00000346103.7:p.Pro151=
ENST00000589115.6:c.453C>T	ENSP00000466872.3:p.Pro151=
ENST00000354171.12:c.453C>T	ENSP00000346103.7:p.Pro151=
ENST00000585480.1:c.186C>T	ENSP00000467900.1:p.Pro62=
ENST00000587648.5:c.333C>T	ENSP00000468349.1:p.Pro111=
ENST00000588919.5:c.372C>T	ENSP00000464989.3:p.Pro124=
ENST00000589115.5:c.453C>T	ENSP00000466872.2:p.Pro151=
ENST00000592940.2:n.392C>T
ENST00000593032.5:c.372C>T	ENSP00000465828.3:p.Pro124=
ENST00000611653.4:c.372C>T	ENSP00000483655.1:p.Pro124=
ENST00000616066.4:c.450C>T	ENSP00000485000.1:p.Pro150=
ENST00000622390.4:c.561C>T	ENSP00000477503.1:p.Pro187=
NM_001039847.2:c.453C>T	NP_001034936.1:p.Pro151=
NM_001039848.2:c.564C>T	NP_001034937.1:p.Pro188=
NM_002085.4:c.453C>T	NP_002076.2:p.Pro151=
NM_001039848.3:c.564C>T	NP_001034937.1:p.Pro188=
NM_001039847.3:c.453C>T	NP_001034936.1:p.Pro151=
NM_001039848.4:c.564C>T	NP_001034937.1:p.Pro188=
NM_001367832.1:c.372C>T	NP_001354761.1:p.Pro124=
NM_002085.5:c.453C>T MANE Select	NP_002076.2:p.Pro151=