Canonical Allele Identifier: CA303992467

Gene: GPX4

Linked Data

• dbSNP Id: rs923701073
• gnomAD v4: 19-1104028-T-C
• MyVariant Identifiers: chr19:g.1104027T>C (hg19) ; chr19:g.1104028T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104028T>C , CM000681.2:g.1104028T>C	GRCh38
NC_000019.9:g.1104027T>C , CM000681.1:g.1104027T>C	GRCh37
NC_000019.8:g.1055027T>C	NCBI36
NG_050621.1:g.5103T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706713.1:c.-16T>C	ENSP00000516510.1:n.-16T>C
ENST00000354171.13:c.-16T>C MANE Select	ENSP00000346103.7:n.-16T>C
ENST00000589115.6:c.-16T>C	ENSP00000466872.3:n.-16T>C
ENST00000354171.12:c.-16T>C	ENSP00000346103.7:n.-16T>C
ENST00000589115.5:c.-16T>C	ENSP00000466872.2:n.-16T>C
ENST00000616066.4:c.-16T>C	ENSP00000485000.1:n.-16T>C
NM_001039847.2:c.-16T>C	NP_001034936.1:n.-16T>C
NM_002085.4:c.-16T>C	NP_002076.2:n.-16T>C
NM_001039847.3:c.-16T>C	NP_001034936.1:n.-16T>C
NM_002085.5:c.-16T>C MANE Select	NP_002076.2:n.-16T>C