Canonical Allele Identifier: CA402940382

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106551G>C (hg19) ; chr19:g.1106552G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106552G>C , CM000681.2:g.1106552G>C	GRCh38
NC_000019.9:g.1106551G>C , CM000681.1:g.1106551G>C	GRCh37
NC_000019.8:g.1057551G>C	NCBI36
NG_050621.1:g.7627G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.685G>C	ENSP00000473614.3:p.Asp229His
ENST00000593032.6:c.554G>C	ENSP00000465828.4:p.Gly185Ala
ENST00000706713.1:c.568G>C	ENSP00000516510.1:p.Asp190His
ENST00000706714.1:c.554G>C	ENSP00000516511.1:p.Gly185Ala
ENST00000706715.1:c.190G>C	ENSP00000516512.1:p.Asp64His
ENST00000354171.13:c.574G>C MANE Select	ENSP00000346103.7:p.Asp192His
ENST00000589115.6:c.*6G>C	ENSP00000466872.3:n.*6G>C
ENST00000354171.12:c.574G>C	ENSP00000346103.7:p.Asp192His
ENST00000585480.1:c.295-21G>C	ENSP00000467900.1:n.295-21G>C
ENST00000587648.5:c.454G>C	ENSP00000468349.1:p.Asp152His
ENST00000588919.5:c.515G>C	ENSP00000464989.3:p.Gly172Ala
ENST00000589115.5:c.*6G>C	ENSP00000466872.2:n.*6G>C
ENST00000592940.2:n.945G>C
ENST00000611653.4:c.493G>C	ENSP00000483655.1:p.Asp165His
ENST00000616066.4:c.571G>C	ENSP00000485000.1:p.Asp191His
ENST00000622390.4:c.682G>C	ENSP00000477503.1:p.Asp228His
NM_001039847.2:c.596G>C	NP_001034936.1:p.Gly199Ala
NM_001039848.2:c.685G>C	NP_001034937.1:p.Asp229His
NM_002085.4:c.574G>C	NP_002076.2:p.Asp192His
NM_001039848.3:c.685G>C	NP_001034937.1:p.Asp229His
NM_001039847.3:c.596G>C	NP_001034936.1:p.Gly199Ala
NM_001039848.4:c.685G>C	NP_001034937.1:p.Asp229His
NM_001367832.1:c.493G>C	NP_001354761.1:p.Asp165His
NM_002085.5:c.574G>C MANE Select	NP_002076.2:p.Asp192His