Canonical Allele Identifier: CA402934136

Gene: GPX4

Linked Data

• MyVariant Identifiers: chr19:g.1104043A>C (hg19) ; chr19:g.1104044A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104044A>C , CM000681.2:g.1104044A>C	GRCh38
NC_000019.9:g.1104043A>C , CM000681.1:g.1104043A>C	GRCh37
NC_000019.8:g.1055043A>C	NCBI36
NG_050621.1:g.5119A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706713.1:c.1A>C	ENSP00000516510.1:p.Met1Leu
ENST00000354171.13:c.1A>C MANE Select	ENSP00000346103.7:p.Met1Leu
ENST00000589115.6:c.1A>C	ENSP00000466872.3:p.Met1Leu
ENST00000354171.12:c.1A>C	ENSP00000346103.7:p.Met1Leu
ENST00000589115.5:c.1A>C	ENSP00000466872.2:p.Met1Leu
ENST00000616066.4:c.1A>C	ENSP00000485000.1:p.Met1Leu
NM_001039847.2:c.1A>C	NP_001034936.1:p.Met1Leu
NM_002085.4:c.1A>C	NP_002076.2:p.Met1Leu
NM_001039847.3:c.1A>C	NP_001034936.1:p.Met1Leu
NM_002085.5:c.1A>C MANE Select	NP_002076.2:p.Met1Leu