Canonical Allele Identifier: CA402934141

Gene: GPX4

Linked Data

• gnomAD v4: 19-1104045-T-C
• MyVariant Identifiers: chr19:g.1104044T>C (hg19) ; chr19:g.1104045T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104045T>C , CM000681.2:g.1104045T>C	GRCh38
NC_000019.9:g.1104044T>C , CM000681.1:g.1104044T>C	GRCh37
NC_000019.8:g.1055044T>C	NCBI36
NG_050621.1:g.5120T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706713.1:c.2T>C	ENSP00000516510.1:p.Met1Thr
ENST00000354171.13:c.2T>C MANE Select	ENSP00000346103.7:p.Met1Thr
ENST00000589115.6:c.2T>C	ENSP00000466872.3:p.Met1Thr
ENST00000354171.12:c.2T>C	ENSP00000346103.7:p.Met1Thr
ENST00000589115.5:c.2T>C	ENSP00000466872.2:p.Met1Thr
ENST00000616066.4:c.2T>C	ENSP00000485000.1:p.Met1Thr
NM_001039847.2:c.2T>C	NP_001034936.1:p.Met1Thr
NM_002085.4:c.2T>C	NP_002076.2:p.Met1Thr
NM_001039847.3:c.2T>C	NP_001034936.1:p.Met1Thr
NM_002085.5:c.2T>C MANE Select	NP_002076.2:p.Met1Thr