Canonical Allele Identifier: CA402937582

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1105750G>C (hg19) ; chr19:g.1105751G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105751G>C , CM000681.2:g.1105751G>C	GRCh38
NC_000019.9:g.1105750G>C , CM000681.1:g.1105750G>C	GRCh37
NC_000019.8:g.1056750G>C	NCBI36
NG_050621.1:g.6826G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.529G>C	ENSP00000473614.3:p.Ala177Pro
ENST00000593032.6:c.337G>C	ENSP00000465828.4:p.Ala113Pro
ENST00000706713.1:c.412G>C	ENSP00000516510.1:p.Ala138Pro
ENST00000706714.1:c.337G>C	ENSP00000516511.1:p.Ala113Pro
ENST00000706715.1:c.34G>C	ENSP00000516512.1:p.Ala12Pro
ENST00000354171.13:c.418G>C MANE Select	ENSP00000346103.7:p.Ala140Pro
ENST00000589115.6:c.418G>C	ENSP00000466872.3:p.Ala140Pro
ENST00000354171.12:c.418G>C	ENSP00000346103.7:p.Ala140Pro
ENST00000585362.6:c.529G>C	ENSP00000473614.2:p.Ala177Pro
ENST00000585480.1:c.151G>C	ENSP00000467900.1:p.Ala51Pro
ENST00000587648.5:c.298G>C	ENSP00000468349.1:p.Ala100Pro
ENST00000588919.5:c.337G>C	ENSP00000464989.3:p.Ala113Pro
ENST00000589115.5:c.418G>C	ENSP00000466872.2:p.Ala140Pro
ENST00000592940.2:n.357G>C
ENST00000593032.5:c.337G>C	ENSP00000465828.3:p.Ala113Pro
ENST00000611653.4:c.337G>C	ENSP00000483655.1:p.Ala113Pro
ENST00000616066.4:c.415G>C	ENSP00000485000.1:p.Ala139Pro
ENST00000622390.4:c.526G>C	ENSP00000477503.1:p.Ala176Pro
NM_001039847.2:c.418G>C	NP_001034936.1:p.Ala140Pro
NM_001039848.2:c.529G>C	NP_001034937.1:p.Ala177Pro
NM_002085.4:c.418G>C	NP_002076.2:p.Ala140Pro
NM_001039848.3:c.529G>C	NP_001034937.1:p.Ala177Pro
NM_001039847.3:c.418G>C	NP_001034936.1:p.Ala140Pro
NM_001039848.4:c.529G>C	NP_001034937.1:p.Ala177Pro
NM_001367832.1:c.337G>C	NP_001354761.1:p.Ala113Pro
NM_002085.5:c.418G>C MANE Select	NP_002076.2:p.Ala140Pro