Canonical Allele Identifier: CA402940649

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1106683A>C (hg19) ; chr19:g.1106684A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106684A>C , CM000681.2:g.1106684A>C	GRCh38
NC_000019.9:g.1106683A>C , CM000681.1:g.1106683A>C	GRCh37
NC_000019.8:g.1057683A>C	NCBI36
NG_050621.1:g.7759A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*112A>C	ENSP00000473614.3:n.*112A>C
ENST00000593032.6:c.686A>C	ENSP00000465828.4:p.Gln229Pro
ENST00000706713.1:c.*112A>C	ENSP00000516510.1:n.*112A>C
ENST00000706714.1:c.686A>C	ENSP00000516511.1:p.Gln229Pro
ENST00000706715.1:c.*112A>C	ENSP00000516512.1:n.*112A>C
ENST00000354171.13:c.*112A>C MANE Select	ENSP00000346103.7:n.*112A>C
ENST00000589115.6:c.*138A>C	ENSP00000466872.3:n.*138A>C
ENST00000354171.12:c.*112A>C	ENSP00000346103.7:n.*112A>C
ENST00000585480.1:c.406A>C	ENSP00000467900.1:p.Ser136Arg
ENST00000588919.5:c.647A>C	ENSP00000464989.3:p.Gln216Pro
ENST00000589115.5:c.*138A>C	ENSP00000466872.2:n.*138A>C
ENST00000592940.2:n.1077A>C
ENST00000611653.4:c.*112A>C	ENSP00000483655.1:n.*112A>C
ENST00000616066.4:c.*112A>C	ENSP00000485000.1:n.*112A>C
ENST00000622390.4:c.*112A>C	ENSP00000477503.1:n.*112A>C
NM_001039847.2:c.*44A>C	NP_001034936.1:n.*44A>C
NM_001039848.2:c.*112A>C	NP_001034937.1:n.*112A>C
NM_002085.4:c.*112A>C	NP_002076.2:n.*112A>C
NM_001039848.3:c.*112A>C	NP_001034937.1:n.*112A>C
NM_001039847.3:c.*44A>C	NP_001034936.1:n.*44A>C
NM_001039848.4:c.*112A>C	NP_001034937.1:n.*112A>C
NM_001367832.1:c.*112A>C	NP_001354761.1:n.*112A>C
NM_002085.5:c.*112A>C MANE Select	NP_002076.2:n.*112A>C