Canonical Allele Identifier: CA402939087

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106241T>C (hg19) ; chr19:g.1106242T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106242T>C , CM000681.2:g.1106242T>C	GRCh38
NC_000019.9:g.1106241T>C , CM000681.1:g.1106241T>C	GRCh37
NC_000019.8:g.1057241T>C	NCBI36
NG_050621.1:g.7317T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588T>C	ENSP00000473614.3:p.Asn196=
ENST00000593032.6:c.457T>C	ENSP00000465828.4:p.Cys153Arg
ENST00000706713.1:c.471T>C	ENSP00000516510.1:p.Asn157=
ENST00000706714.1:c.457T>C	ENSP00000516511.1:p.Cys153Arg
ENST00000706715.1:c.93T>C	ENSP00000516512.1:p.Asn31=
ENST00000354171.13:c.477T>C MANE Select	ENSP00000346103.7:p.Asn159=
ENST00000589115.6:c.477-158T>C	ENSP00000466872.3:n.477-158T>C
ENST00000354171.12:c.477T>C	ENSP00000346103.7:p.Asn159=
ENST00000585480.1:c.210T>C	ENSP00000467900.1:p.Asn70=
ENST00000587648.5:c.357T>C	ENSP00000468349.1:p.Asn119=
ENST00000588919.5:c.396T>C	ENSP00000464989.3:p.Asn132=
ENST00000589115.5:c.477-158T>C	ENSP00000466872.2:n.477-158T>C
ENST00000592940.2:n.848T>C
ENST00000593032.5:c.457T>C	ENSP00000465828.3:p.Cys153Arg
ENST00000611653.4:c.396T>C	ENSP00000483655.1:p.Asn132=
ENST00000616066.4:c.474T>C	ENSP00000485000.1:p.Asn158=
ENST00000622390.4:c.585T>C	ENSP00000477503.1:p.Asn195=
NM_001039847.2:c.477T>C	NP_001034936.1:p.Asn159=
NM_001039848.2:c.588T>C	NP_001034937.1:p.Asn196=
NM_002085.4:c.477T>C	NP_002076.2:p.Asn159=
NM_001039848.3:c.588T>C	NP_001034937.1:p.Asn196=
NM_001039847.3:c.477T>C	NP_001034936.1:p.Asn159=
NM_001039848.4:c.588T>C	NP_001034937.1:p.Asn196=
NM_001367832.1:c.396T>C	NP_001354761.1:p.Asn132=
NM_002085.5:c.477T>C MANE Select	NP_002076.2:p.Asn159=