Canonical Allele Identifier: CA2317519280
Gene: GPX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104443_1104465delinsGGGGGTCCAGGCTTGCAGGGGGC , CM000681.2:g.1104443_1104465delinsGGGGGTCCAGGCTTGCAGGGGGC GRCh38
NC_000019.9:g.1104442_1104464delinsGGGGGTCCAGGCTTGCAGGGGGC , CM000681.1:g.1104442_1104464delinsGGGGGTCCAGGCTTGCAGGGGGC GRCh37
NC_000019.8:g.1055442_1055464delinsGGGGGTCCAGGCTTGCAGGGGGC NCBI36
NG_050621.1:g.5518_5540delinsGGGGGTCCAGGCTTGCAGGGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000593032.6:c.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000465828.4:n.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC
ENST00000706713.1:c.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000516510.1:n.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGG...
ENST00000706714.1:c.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000516511.1:n.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC
ENST00000706715.1:c.-301+115_-301+137delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000516512.1:n.-301+115_-301+137delinsGGGGGTCCAGGCTTGCAG...
ENST00000354171.13:c.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC MANE Select ENSP00000346103.7:n.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGG...
ENST00000589115.6:c.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000466872.3:n.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGG...
ENST00000354171.12:c.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000346103.7:n.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGG...
ENST00000585362.6:c.-292_-270delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000473614.2:n.-292_-270delinsGGGGGTCCAGGCTTGCAGGGGGC
ENST00000588919.5:c.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000464989.3:n.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC
ENST00000589115.5:c.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000466872.2:n.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGG...
ENST00000593032.5:c.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000465828.3:n.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC
ENST00000611653.4:c.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000483655.1:n.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC
ENST00000616066.4:c.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC ENSP00000485000.1:n.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGG...
NM_001039847.2:c.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC NP_001034936.1:n.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC
NM_002085.4:c.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC NP_002076.2:n.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC
NM_001039847.3:c.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC NP_001034936.1:n.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC
NM_001367832.1:c.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC NP_001354761.1:n.3+316_3+338delinsGGGGGTCCAGGCTTGCAGGGGGC
NM_002085.5:c.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC MANE Select NP_002076.2:n.84+316_84+338delinsGGGGGTCCAGGCTTGCAGGGGGC