Canonical Allele Identifier: CA402939755

Gene: GPX4

Linked Data

• dbSNP Id: rs1192146377
• gnomAD v2: 19-1106410-C-T
• gnomAD v4: 19-1106411-C-T
• MyVariant Identifiers: chr19:g.1106410C>T (hg19) ; chr19:g.1106411C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106411C>T , CM000681.2:g.1106411C>T	GRCh38
NC_000019.9:g.1106410C>T , CM000681.1:g.1106410C>T	GRCh37
NC_000019.8:g.1057410C>T	NCBI36
NG_050621.1:g.7486C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.624C>T	ENSP00000473614.3:p.Asp208=
ENST00000593032.6:c.493C>T	ENSP00000465828.4:p.Gln165Ter
ENST00000706713.1:c.507C>T	ENSP00000516510.1:p.Asp169=
ENST00000706714.1:c.493C>T	ENSP00000516511.1:p.Gln165Ter
ENST00000706715.1:c.129C>T	ENSP00000516512.1:p.Asp43=
ENST00000354171.13:c.513C>T MANE Select	ENSP00000346103.7:p.Asp171=
ENST00000589115.6:c.488C>T	ENSP00000466872.3:p.Thr163Ile
ENST00000354171.12:c.513C>T	ENSP00000346103.7:p.Asp171=
ENST00000585480.1:c.246C>T	ENSP00000467900.1:p.Asp82=
ENST00000587648.5:c.393C>T	ENSP00000468349.1:p.Asp131=
ENST00000588919.5:c.454C>T	ENSP00000464989.3:p.Gln152Ter
ENST00000589115.5:c.488C>T	ENSP00000466872.2:p.Thr163Ile
ENST00000592940.2:n.884C>T
ENST00000593032.5:c.493C>T	ENSP00000465828.3:p.Gln165Ter
ENST00000611653.4:c.432C>T	ENSP00000483655.1:p.Asp144=
ENST00000616066.4:c.510C>T	ENSP00000485000.1:p.Asp170=
ENST00000622390.4:c.621C>T	ENSP00000477503.1:p.Asp207=
NM_001039847.2:c.535C>T	NP_001034936.1:p.Gln179Ter
NM_001039848.2:c.624C>T	NP_001034937.1:p.Asp208=
NM_002085.4:c.513C>T	NP_002076.2:p.Asp171=
NM_001039848.3:c.624C>T	NP_001034937.1:p.Asp208=
NM_001039847.3:c.535C>T	NP_001034936.1:p.Gln179Ter
NM_001039848.4:c.624C>T	NP_001034937.1:p.Asp208=
NM_001367832.1:c.432C>T	NP_001354761.1:p.Asp144=
NM_002085.5:c.513C>T MANE Select	NP_002076.2:p.Asp171=