Canonical Allele Identifier: CA2317520427
Gene: GPX4 HGNC NCBI

Linked Data

dbSNP Id: rs2079650718

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1106128_1106129del , CM000681.2:g.1106128_1106129del GRCh38
NC_000019.9:g.1106127_1106128del , CM000681.1:g.1106127_1106128del GRCh37
NC_000019.8:g.1057127_1057128del NCBI36
NG_050621.1:g.7203_7204del

Transcript Alleles

HGVS Amino-acid Change
ENST00000585362.7:c.588-114_588-113del ENSP00000473614.3:n.588-114_588-113del
ENST00000593032.6:c.396-53_396-52del ENSP00000465828.4:n.396-53_396-52del
ENST00000706713.1:c.471-114_471-113del ENSP00000516510.1:n.471-114_471-113del
ENST00000706714.1:c.396-53_396-52del ENSP00000516511.1:n.396-53_396-52del
ENST00000706715.1:c.93-114_93-113del ENSP00000516512.1:n.93-114_93-113del
ENST00000354171.13:c.477-114_477-113del MANE Select ENSP00000346103.7:n.477-114_477-113del
ENST00000589115.6:c.477-272_477-271del ENSP00000466872.3:n.477-272_477-271del
ENST00000354171.12:c.477-114_477-113del ENSP00000346103.7:n.477-114_477-113del
ENST00000585480.1:c.210-114_210-113del ENSP00000467900.1:n.210-114_210-113del
ENST00000587648.5:c.357-114_357-113del ENSP00000468349.1:n.357-114_357-113del
ENST00000588919.5:c.396-114_396-113del ENSP00000464989.3:n.396-114_396-113del
ENST00000589115.5:c.477-272_477-271del ENSP00000466872.2:n.477-272_477-271del
ENST00000592940.2:n.734_735del
ENST00000593032.5:c.396-53_396-52del ENSP00000465828.3:n.396-53_396-52del
ENST00000611653.4:c.396-114_396-113del ENSP00000483655.1:n.396-114_396-113del
ENST00000616066.4:c.474-114_474-113del ENSP00000485000.1:n.474-114_474-113del
ENST00000622390.4:c.585-114_585-113del ENSP00000477503.1:n.585-114_585-113del
NM_001039847.2:c.477-114_477-113del NP_001034936.1:n.477-114_477-113del
NM_001039848.2:c.588-114_588-113del NP_001034937.1:n.588-114_588-113del
NM_002085.4:c.477-114_477-113del NP_002076.2:n.477-114_477-113del
NM_001039848.3:c.588-114_588-113del NP_001034937.1:n.588-114_588-113del
NM_001039847.3:c.477-114_477-113del NP_001034936.1:n.477-114_477-113del
NM_001039848.4:c.588-114_588-113del NP_001034937.1:n.588-114_588-113del
NM_001367832.1:c.396-114_396-113del NP_001354761.1:n.396-114_396-113del
NM_002085.5:c.477-114_477-113del MANE Select NP_002076.2:n.477-114_477-113del