Canonical Allele Identifier: CA2588207663
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106094_1106174del , CM000681.2:g.1106094_1106174del GRCh38
NC_000019.9:g.1106093_1106173del , CM000681.1:g.1106093_1106173del GRCh37
NC_000019.8:g.1057093_1057173del NCBI36
NG_050621.1:g.7169_7249del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.588-148_588-68del ENSP00000473614.3:n.588-148_588-68del
ENST00000593032.6:c.396-87_396-7del ENSP00000465828.4:n.396-87_396-7del
ENST00000706713.1:c.471-148_471-68del ENSP00000516510.1:n.471-148_471-68del
ENST00000706714.1:c.396-87_396-7del ENSP00000516511.1:n.396-87_396-7del
ENST00000706715.1:c.93-148_93-68del ENSP00000516512.1:n.93-148_93-68del
ENST00000354171.13:c.477-148_477-68del MANE Select ENSP00000346103.7:n.477-148_477-68del
ENST00000589115.6:c.476+285_477-226del ENSP00000466872.3:n.476+285_477-226del
ENST00000354171.12:c.477-148_477-68del ENSP00000346103.7:n.477-148_477-68del
ENST00000585480.1:c.210-148_210-68del ENSP00000467900.1:n.210-148_210-68del
ENST00000587648.5:c.357-148_357-68del ENSP00000468349.1:n.357-148_357-68del
ENST00000588919.5:c.396-148_396-68del ENSP00000464989.3:n.396-148_396-68del
ENST00000589115.5:c.476+285_477-226del ENSP00000466872.2:n.476+285_477-226del
ENST00000592940.2:n.700_780del
ENST00000593032.5:c.396-87_396-7del ENSP00000465828.3:n.396-87_396-7del
ENST00000611653.4:c.396-148_396-68del ENSP00000483655.1:n.396-148_396-68del
ENST00000616066.4:c.474-148_474-68del ENSP00000485000.1:n.474-148_474-68del
ENST00000622390.4:c.585-148_585-68del ENSP00000477503.1:n.585-148_585-68del
NM_001039847.2:c.477-148_477-68del NP_001034936.1:n.477-148_477-68del
NM_001039848.2:c.588-148_588-68del NP_001034937.1:n.588-148_588-68del
NM_002085.4:c.477-148_477-68del NP_002076.2:n.477-148_477-68del
NM_001039848.3:c.588-148_588-68del NP_001034937.1:n.588-148_588-68del
NM_001039847.3:c.477-148_477-68del NP_001034936.1:n.477-148_477-68del
NM_001039848.4:c.588-148_588-68del NP_001034937.1:n.588-148_588-68del
NM_001367832.1:c.396-148_396-68del NP_001354761.1:n.396-148_396-68del
NM_002085.5:c.477-148_477-68del MANE Select NP_002076.2:n.477-148_477-68del