Canonical Allele Identifier: CA631018524

Gene: GPX4

Linked Data

• dbSNP Id: rs1206770698
• gnomAD v2: 19-1104030-C-T
• gnomAD v4: 19-1104031-C-T
• MyVariant Identifiers: chr19:g.1104030C>T (hg19) ; chr19:g.1104031C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104031C>T , CM000681.2:g.1104031C>T	GRCh38
NC_000019.9:g.1104030C>T , CM000681.1:g.1104030C>T	GRCh37
NC_000019.8:g.1055030C>T	NCBI36
NG_050621.1:g.5106C>T

Transcript Alleles

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