Canonical Allele Identifier: CA631018918

Gene: GPX4

Linked Data

• dbSNP Id: rs3177111
• gnomAD v2: 19-1106779-C-T
• gnomAD v3: 19-1106780-C-T
• gnomAD v4: 19-1106780-C-T
• MyVariant Identifiers: chr19:g.1106779C>T (hg19) ; chr19:g.1106780C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106780C>T , CM000681.2:g.1106780C>T	GRCh38
NC_000019.9:g.1106779C>T , CM000681.1:g.1106779C>T	GRCh37
NC_000019.8:g.1057779C>T	NCBI36
NG_050621.1:g.7855C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706713.1:c.*208C>T	ENSP00000516510.1:n.*208C>T
ENST00000354171.12:c.*208C>T	ENSP00000346103.7:n.*208C>T
ENST00000588919.5:c.*14C>T	ENSP00000464989.3:n.*14C>T
ENST00000592940.2:n.1173C>T
ENST00000616066.4:c.*208C>T	ENSP00000485000.1:n.*208C>T
ENST00000622390.4:c.*208C>T	ENSP00000477503.1:n.*208C>T
NM_001039847.2:c.*140C>T	NP_001034936.1:n.*140C>T
NM_001039848.2:c.*208C>T	NP_001034937.1:n.*208C>T
NM_002085.4:c.*208C>T	NP_002076.2:n.*208C>T
NM_001039848.3:c.*208C>T	NP_001034937.1:n.*208C>T