Canonical Allele Identifier: CA2576545152
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106228_1106229del , CM000681.2:g.1106228_1106229del GRCh38
NC_000019.9:g.1106227_1106228del , CM000681.1:g.1106227_1106228del GRCh37
NC_000019.8:g.1057227_1057228del NCBI36
NG_050621.1:g.7303_7304del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.588-14_588-13del ENSP00000473614.3:n.588-14_588-13del
ENST00000593032.6:c.443_444del ENSP00000465828.4:p.Val148AlafsTer23
ENST00000706713.1:c.471-14_471-13del ENSP00000516510.1:n.471-14_471-13del
ENST00000706714.1:c.443_444del ENSP00000516511.1:p.Val148AlafsTer23
ENST00000706715.1:c.93-14_93-13del ENSP00000516512.1:n.93-14_93-13del
ENST00000354171.13:c.477-14_477-13del MANE Select ENSP00000346103.7:n.477-14_477-13del
ENST00000589115.6:c.477-172_477-171del ENSP00000466872.3:n.477-172_477-171del
ENST00000354171.12:c.477-14_477-13del ENSP00000346103.7:n.477-14_477-13del
ENST00000585480.1:c.210-14_210-13del ENSP00000467900.1:n.210-14_210-13del
ENST00000587648.5:c.357-14_357-13del ENSP00000468349.1:n.357-14_357-13del
ENST00000588919.5:c.396-14_396-13del ENSP00000464989.3:n.396-14_396-13del
ENST00000589115.5:c.477-172_477-171del ENSP00000466872.2:n.477-172_477-171del
ENST00000592940.2:n.834_835del
ENST00000593032.5:c.443_444del ENSP00000465828.3:p.Val148AlafsTer23
ENST00000611653.4:c.396-14_396-13del ENSP00000483655.1:n.396-14_396-13del
ENST00000616066.4:c.474-14_474-13del ENSP00000485000.1:n.474-14_474-13del
ENST00000622390.4:c.585-14_585-13del ENSP00000477503.1:n.585-14_585-13del
NM_001039847.2:c.477-14_477-13del NP_001034936.1:n.477-14_477-13del
NM_001039848.2:c.588-14_588-13del NP_001034937.1:n.588-14_588-13del
NM_002085.4:c.477-14_477-13del NP_002076.2:n.477-14_477-13del
NM_001039848.3:c.588-14_588-13del NP_001034937.1:n.588-14_588-13del
NM_001039847.3:c.477-14_477-13del NP_001034936.1:n.477-14_477-13del
NM_001039848.4:c.588-14_588-13del NP_001034937.1:n.588-14_588-13del
NM_001367832.1:c.396-14_396-13del NP_001354761.1:n.396-14_396-13del
NM_002085.5:c.477-14_477-13del MANE Select NP_002076.2:n.477-14_477-13del