Canonical Allele Identifier: CA402934163

Gene: GPX4

Linked Data

• gnomAD v4: 19-1104057-G-T
• MyVariant Identifiers: chr19:g.1104056G>T (hg19) ; chr19:g.1104057G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104057G>T , CM000681.2:g.1104057G>T	GRCh38
NC_000019.9:g.1104056G>T , CM000681.1:g.1104056G>T	GRCh37
NC_000019.8:g.1055056G>T	NCBI36
NG_050621.1:g.5132G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706713.1:c.14G>T	ENSP00000516510.1:p.Arg5Leu
ENST00000354171.13:c.14G>T MANE Select	ENSP00000346103.7:p.Arg5Leu
ENST00000589115.6:c.14G>T	ENSP00000466872.3:p.Arg5Leu
ENST00000354171.12:c.14G>T	ENSP00000346103.7:p.Arg5Leu
ENST00000589115.5:c.14G>T	ENSP00000466872.2:p.Arg5Leu
ENST00000611653.4:c.-68G>T	ENSP00000483655.1:n.-68G>T
ENST00000616066.4:c.14G>T	ENSP00000485000.1:p.Arg5Leu
NM_001039847.2:c.14G>T	NP_001034936.1:p.Arg5Leu
NM_002085.4:c.14G>T	NP_002076.2:p.Arg5Leu
NM_001039847.3:c.14G>T	NP_001034936.1:p.Arg5Leu
NM_001367832.1:c.-68G>T	NP_001354761.1:n.-68G>T
NM_002085.5:c.14G>T MANE Select	NP_002076.2:p.Arg5Leu