Canonical Allele Identifier: CA402937574

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105745A>C (hg19) ; chr19:g.1105746A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105746A>C , CM000681.2:g.1105746A>C	GRCh38
NC_000019.9:g.1105745A>C , CM000681.1:g.1105745A>C	GRCh37
NC_000019.8:g.1056745A>C	NCBI36
NG_050621.1:g.6821A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.524A>C	ENSP00000473614.3:p.Asp175Ala
ENST00000593032.6:c.332A>C	ENSP00000465828.4:p.Asp111Ala
ENST00000706713.1:c.407A>C	ENSP00000516510.1:p.Asp136Ala
ENST00000706714.1:c.332A>C	ENSP00000516511.1:p.Asp111Ala
ENST00000706715.1:c.29A>C	ENSP00000516512.1:p.Asp10Ala
ENST00000354171.13:c.413A>C MANE Select	ENSP00000346103.7:p.Asp138Ala
ENST00000589115.6:c.413A>C	ENSP00000466872.3:p.Asp138Ala
ENST00000354171.12:c.413A>C	ENSP00000346103.7:p.Asp138Ala
ENST00000585362.6:c.524A>C	ENSP00000473614.2:p.Asp175Ala
ENST00000585480.1:c.146A>C	ENSP00000467900.1:p.Asp49Ala
ENST00000587648.5:c.293A>C	ENSP00000468349.1:p.Asp98Ala
ENST00000588919.5:c.332A>C	ENSP00000464989.3:p.Asp111Ala
ENST00000589115.5:c.413A>C	ENSP00000466872.2:p.Asp138Ala
ENST00000592940.2:n.352A>C
ENST00000593032.5:c.332A>C	ENSP00000465828.3:p.Asp111Ala
ENST00000611653.4:c.332A>C	ENSP00000483655.1:p.Asp111Ala
ENST00000616066.4:c.410A>C	ENSP00000485000.1:p.Asp137Ala
ENST00000622390.4:c.521A>C	ENSP00000477503.1:p.Asp174Ala
NM_001039847.2:c.413A>C	NP_001034936.1:p.Asp138Ala
NM_001039848.2:c.524A>C	NP_001034937.1:p.Asp175Ala
NM_002085.4:c.413A>C	NP_002076.2:p.Asp138Ala
NM_001039848.3:c.524A>C	NP_001034937.1:p.Asp175Ala
NM_001039847.3:c.413A>C	NP_001034936.1:p.Asp138Ala
NM_001039848.4:c.524A>C	NP_001034937.1:p.Asp175Ala
NM_001367832.1:c.332A>C	NP_001354761.1:p.Asp111Ala
NM_002085.5:c.413A>C MANE Select	NP_002076.2:p.Asp138Ala