Canonical Allele Identifier: CA631018525

Gene: GPX4

Linked Data

• dbSNP Id: rs1274743142
• gnomAD v2: 19-1104031-A-T
• gnomAD v4: 19-1104032-A-T
• MyVariant Identifiers: chr19:g.1104031A>T (hg19) ; chr19:g.1104032A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104032A>T , CM000681.2:g.1104032A>T	GRCh38
NC_000019.9:g.1104031A>T , CM000681.1:g.1104031A>T	GRCh37
NC_000019.8:g.1055031A>T	NCBI36
NG_050621.1:g.5107A>T

Transcript Alleles

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