Canonical Allele Identifier: CA402940758

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106741-C-A
• MyVariant Identifiers: chr19:g.1106740C>A (hg19) ; chr19:g.1106741C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106741C>A , CM000681.2:g.1106741C>A	GRCh38
NC_000019.9:g.1106740C>A , CM000681.1:g.1106740C>A	GRCh37
NC_000019.8:g.1057740C>A	NCBI36
NG_050621.1:g.7816C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*169C>A	ENSP00000473614.3:n.*169C>A
ENST00000593032.6:c.743C>A	ENSP00000465828.4:p.Pro248Gln
ENST00000706713.1:c.*169C>A	ENSP00000516510.1:n.*169C>A
ENST00000706714.1:c.743C>A	ENSP00000516511.1:p.Pro248Gln
ENST00000706715.1:c.*169C>A	ENSP00000516512.1:n.*169C>A
ENST00000354171.13:c.*169C>A MANE Select	ENSP00000346103.7:n.*169C>A
ENST00000589115.6:c.*195C>A	ENSP00000466872.3:n.*195C>A
ENST00000354171.12:c.*169C>A	ENSP00000346103.7:n.*169C>A
ENST00000585480.1:c.463C>A	ENSP00000467900.1:p.His155Asn
ENST00000588919.5:c.704C>A	ENSP00000464989.3:p.Pro235Gln
ENST00000589115.5:c.*195C>A	ENSP00000466872.2:n.*195C>A
ENST00000592940.2:n.1134C>A
ENST00000611653.4:c.*169C>A	ENSP00000483655.1:n.*169C>A
ENST00000616066.4:c.*169C>A	ENSP00000485000.1:n.*169C>A
ENST00000622390.4:c.*169C>A	ENSP00000477503.1:n.*169C>A
NM_001039847.2:c.*101C>A	NP_001034936.1:n.*101C>A
NM_001039848.2:c.*169C>A	NP_001034937.1:n.*169C>A
NM_002085.4:c.*169C>A	NP_002076.2:n.*169C>A
NM_001039848.3:c.*169C>A	NP_001034937.1:n.*169C>A
NM_001039847.3:c.*101C>A	NP_001034936.1:n.*101C>A
NM_001039848.4:c.*169C>A	NP_001034937.1:n.*169C>A
NM_001367832.1:c.*169C>A	NP_001354761.1:n.*169C>A
NM_002085.5:c.*169C>A MANE Select	NP_002076.2:n.*169C>A