Canonical Allele Identifier: CA783222371

Gene: GPX4

Linked Data

• dbSNP Id: rs1362380173
• MyVariant Identifiers: chr19:g.1103959_1103960insG (hg19) ; chr19:g.1103960_1103961insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1103963dup , CM000681.2:g.1103963dup	GRCh38
NC_000019.9:g.1103962dup , CM000681.1:g.1103962dup	GRCh37
NC_000019.8:g.1054962dup	NCBI36
NG_050621.1:g.5038dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354171.12:c.-81dup	ENSP00000346103.7:n.-81dup
ENST00000616066.4:c.-81dup	ENSP00000485000.1:n.-81dup
NM_001039847.2:c.-81dup	NP_001034936.1:n.-81dup
NM_002085.4:c.-81dup	NP_002076.2:n.-81dup