Canonical Allele Identifier: CA303992547

Gene: GPX4

Linked Data

• dbSNP Id: rs772251077
• gnomAD v2: 19-1104052-G-C
• gnomAD v3: 19-1104053-G-C
• gnomAD v4: 19-1104053-G-C
• MyVariant Identifiers: chr19:g.1104052G>C (hg19) ; chr19:g.1104053G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104053G>C , CM000681.2:g.1104053G>C	GRCh38
NC_000019.9:g.1104052G>C , CM000681.1:g.1104052G>C	GRCh37
NC_000019.8:g.1055052G>C	NCBI36
NG_050621.1:g.5128G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706713.1:c.10G>C	ENSP00000516510.1:p.Gly4Arg
ENST00000354171.13:c.10G>C MANE Select	ENSP00000346103.7:p.Gly4Arg
ENST00000589115.6:c.10G>C	ENSP00000466872.3:p.Gly4Arg
ENST00000354171.12:c.10G>C	ENSP00000346103.7:p.Gly4Arg
ENST00000589115.5:c.10G>C	ENSP00000466872.2:p.Gly4Arg
ENST00000611653.4:c.-72G>C	ENSP00000483655.1:n.-72G>C
ENST00000616066.4:c.10G>C	ENSP00000485000.1:p.Gly4Arg
NM_001039847.2:c.10G>C	NP_001034936.1:p.Gly4Arg
NM_002085.4:c.10G>C	NP_002076.2:p.Gly4Arg
NM_001039847.3:c.10G>C	NP_001034936.1:p.Gly4Arg
NM_002085.5:c.10G>C MANE Select	NP_002076.2:p.Gly4Arg