Canonical Allele Identifier: CA402939842

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106415A>G (hg19) ; chr19:g.1106416A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106416A>G , CM000681.2:g.1106416A>G	GRCh38
NC_000019.9:g.1106415A>G , CM000681.1:g.1106415A>G	GRCh37
NC_000019.8:g.1057415A>G	NCBI36
NG_050621.1:g.7491A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.629A>G	ENSP00000473614.3:p.Asn210Ser
ENST00000593032.6:c.498A>G	ENSP00000465828.4:p.Glu166=
ENST00000706713.1:c.512A>G	ENSP00000516510.1:p.Asn171Ser
ENST00000706714.1:c.498A>G	ENSP00000516511.1:p.Glu166=
ENST00000706715.1:c.134A>G	ENSP00000516512.1:p.Asn45Ser
ENST00000354171.13:c.518A>G MANE Select	ENSP00000346103.7:p.Asn173Ser
ENST00000589115.6:c.493A>G	ENSP00000466872.3:p.Thr165Ala
ENST00000354171.12:c.518A>G	ENSP00000346103.7:p.Asn173Ser
ENST00000585480.1:c.251A>G	ENSP00000467900.1:p.Asn84Ser
ENST00000587648.5:c.398A>G	ENSP00000468349.1:p.Asn133Ser
ENST00000588919.5:c.459A>G	ENSP00000464989.3:p.Glu153=
ENST00000589115.5:c.493A>G	ENSP00000466872.2:p.Thr165Ala
ENST00000592940.2:n.889A>G
ENST00000593032.5:c.498A>G	ENSP00000465828.3:p.Glu166=
ENST00000611653.4:c.437A>G	ENSP00000483655.1:p.Asn146Ser
ENST00000616066.4:c.515A>G	ENSP00000485000.1:p.Asn172Ser
ENST00000622390.4:c.626A>G	ENSP00000477503.1:p.Asn209Ser
NM_001039847.2:c.540A>G	NP_001034936.1:p.Glu180=
NM_001039848.2:c.629A>G	NP_001034937.1:p.Asn210Ser
NM_002085.4:c.518A>G	NP_002076.2:p.Asn173Ser
NM_001039848.3:c.629A>G	NP_001034937.1:p.Asn210Ser
NM_001039847.3:c.540A>G	NP_001034936.1:p.Glu180=
NM_001039848.4:c.629A>G	NP_001034937.1:p.Asn210Ser
NM_001367832.1:c.437A>G	NP_001354761.1:p.Asn146Ser
NM_002085.5:c.518A>G MANE Select	NP_002076.2:p.Asn173Ser