Canonical Allele Identifier: CA402939198

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106257-C-A
• MyVariant Identifiers: chr19:g.1106256C>A (hg19) ; chr19:g.1106257C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106257C>A , CM000681.2:g.1106257C>A	GRCh38
NC_000019.9:g.1106256C>A , CM000681.1:g.1106256C>A	GRCh37
NC_000019.8:g.1057256C>A	NCBI36
NG_050621.1:g.7332C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.603C>A	ENSP00000473614.3:p.Asn201Lys
ENST00000593032.6:c.472C>A	ENSP00000465828.4:p.Leu158Ile
ENST00000706713.1:c.486C>A	ENSP00000516510.1:p.Asn162Lys
ENST00000706714.1:c.472C>A	ENSP00000516511.1:p.Leu158Ile
ENST00000706715.1:c.108C>A	ENSP00000516512.1:p.Asn36Lys
ENST00000354171.13:c.492C>A MANE Select	ENSP00000346103.7:p.Asn164Lys
ENST00000589115.6:c.477-143C>A	ENSP00000466872.3:n.477-143C>A
ENST00000354171.12:c.492C>A	ENSP00000346103.7:p.Asn164Lys
ENST00000585480.1:c.225C>A	ENSP00000467900.1:p.Asn75Lys
ENST00000587648.5:c.372C>A	ENSP00000468349.1:p.Asn124Lys
ENST00000588919.5:c.411C>A	ENSP00000464989.3:p.Asn137Lys
ENST00000589115.5:c.477-143C>A	ENSP00000466872.2:n.477-143C>A
ENST00000592940.2:n.863C>A
ENST00000593032.5:c.472C>A	ENSP00000465828.3:p.Leu158Ile
ENST00000611653.4:c.411C>A	ENSP00000483655.1:p.Asn137Lys
ENST00000616066.4:c.489C>A	ENSP00000485000.1:p.Asn163Lys
ENST00000622390.4:c.600C>A	ENSP00000477503.1:p.Asn200Lys
NM_001039847.2:c.492C>A	NP_001034936.1:p.Asn164Lys
NM_001039848.2:c.603C>A	NP_001034937.1:p.Asn201Lys
NM_002085.4:c.492C>A	NP_002076.2:p.Asn164Lys
NM_001039848.3:c.603C>A	NP_001034937.1:p.Asn201Lys
NM_001039847.3:c.492C>A	NP_001034936.1:p.Asn164Lys
NM_001039848.4:c.603C>A	NP_001034937.1:p.Asn201Lys
NM_001367832.1:c.411C>A	NP_001354761.1:p.Asn137Lys
NM_002085.5:c.492C>A MANE Select	NP_002076.2:p.Asn164Lys