Canonical Allele Identifier: CA9037586

Gene: GPX4

Linked Data

• dbSNP Id: rs144677581
• ExAC: 19:1106787 A / T
• gnomAD v2: 19-1106787-A-T
• gnomAD v3: 19-1106788-A-T
• gnomAD v4: 19-1106788-A-T
• MyVariant Identifiers: chr19:g.1106787A>T (hg19) ; chr19:g.1106788A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106788A>T , CM000681.2:g.1106788A>T	GRCh38
NC_000019.9:g.1106787A>T , CM000681.1:g.1106787A>T	GRCh37
NC_000019.8:g.1057787A>T	NCBI36
NG_050621.1:g.7863A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354171.12:c.*216A>T	ENSP00000346103.7:n.*216A>T
ENST00000588919.5:c.*22A>T	ENSP00000464989.3:n.*22A>T
ENST00000592940.2:n.1181A>T
NM_001039847.2:c.*148A>T	NP_001034936.1:n.*148A>T
NM_001039848.2:c.*216A>T	NP_001034937.1:n.*216A>T
NM_002085.4:c.*216A>T	NP_002076.2:n.*216A>T
NM_001039848.3:c.*216A>T	NP_001034937.1:n.*216A>T