Canonical Allele Identifier: CA402939191

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106255A>C (hg19) ; chr19:g.1106256A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106256A>C , CM000681.2:g.1106256A>C	GRCh38
NC_000019.9:g.1106255A>C , CM000681.1:g.1106255A>C	GRCh37
NC_000019.8:g.1057255A>C	NCBI36
NG_050621.1:g.7331A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.602A>C	ENSP00000473614.3:p.Asn201Thr
ENST00000593032.6:c.471A>C	ENSP00000465828.4:p.Glu157Asp
ENST00000706713.1:c.485A>C	ENSP00000516510.1:p.Asn162Thr
ENST00000706714.1:c.471A>C	ENSP00000516511.1:p.Glu157Asp
ENST00000706715.1:c.107A>C	ENSP00000516512.1:p.Asn36Thr
ENST00000354171.13:c.491A>C MANE Select	ENSP00000346103.7:p.Asn164Thr
ENST00000589115.6:c.477-144A>C	ENSP00000466872.3:n.477-144A>C
ENST00000354171.12:c.491A>C	ENSP00000346103.7:p.Asn164Thr
ENST00000585480.1:c.224A>C	ENSP00000467900.1:p.Asn75Thr
ENST00000587648.5:c.371A>C	ENSP00000468349.1:p.Asn124Thr
ENST00000588919.5:c.410A>C	ENSP00000464989.3:p.Asn137Thr
ENST00000589115.5:c.477-144A>C	ENSP00000466872.2:n.477-144A>C
ENST00000592940.2:n.862A>C
ENST00000593032.5:c.471A>C	ENSP00000465828.3:p.Glu157Asp
ENST00000611653.4:c.410A>C	ENSP00000483655.1:p.Asn137Thr
ENST00000616066.4:c.488A>C	ENSP00000485000.1:p.Asn163Thr
ENST00000622390.4:c.599A>C	ENSP00000477503.1:p.Asn200Thr
NM_001039847.2:c.491A>C	NP_001034936.1:p.Asn164Thr
NM_001039848.2:c.602A>C	NP_001034937.1:p.Asn201Thr
NM_002085.4:c.491A>C	NP_002076.2:p.Asn164Thr
NM_001039848.3:c.602A>C	NP_001034937.1:p.Asn201Thr
NM_001039847.3:c.491A>C	NP_001034936.1:p.Asn164Thr
NM_001039848.4:c.602A>C	NP_001034937.1:p.Asn201Thr
NM_001367832.1:c.410A>C	NP_001354761.1:p.Asn137Thr
NM_002085.5:c.491A>C MANE Select	NP_002076.2:p.Asn164Thr