Canonical Allele Identifier: CA2588206006
Gene: GPX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104258_1104263del , CM000681.2:g.1104258_1104263del GRCh38
NC_000019.9:g.1104257_1104262del , CM000681.1:g.1104257_1104262del GRCh37
NC_000019.8:g.1055257_1055262del NCBI36
NG_050621.1:g.5333_5338del

Transcript Alleles

HGVS Amino-acid Change
ENST00000593032.6:c.3+131_3+136del ENSP00000465828.4:n.3+131_3+136del
ENST00000706713.1:c.84+131_84+136del ENSP00000516510.1:n.84+131_84+136del
ENST00000706714.1:c.3+131_3+136del ENSP00000516511.1:n.3+131_3+136del
ENST00000706715.1:c.-371_-366del ENSP00000516512.1:n.-371_-366del
ENST00000354171.13:c.84+131_84+136del MANE Select ENSP00000346103.7:n.84+131_84+136del
ENST00000589115.6:c.84+131_84+136del ENSP00000466872.3:n.84+131_84+136del
ENST00000354171.12:c.84+131_84+136del ENSP00000346103.7:n.84+131_84+136del
ENST00000588919.5:c.3+131_3+136del ENSP00000464989.3:n.3+131_3+136del
ENST00000589115.5:c.84+131_84+136del ENSP00000466872.2:n.84+131_84+136del
ENST00000593032.5:c.3+131_3+136del ENSP00000465828.3:n.3+131_3+136del
ENST00000611653.4:c.3+131_3+136del ENSP00000483655.1:n.3+131_3+136del
ENST00000616066.4:c.84+131_84+136del ENSP00000485000.1:n.84+131_84+136del
NM_001039847.2:c.84+131_84+136del NP_001034936.1:n.84+131_84+136del
NM_002085.4:c.84+131_84+136del NP_002076.2:n.84+131_84+136del
NM_001039847.3:c.84+131_84+136del NP_001034936.1:n.84+131_84+136del
NM_001367832.1:c.3+131_3+136del NP_001354761.1:n.3+131_3+136del
NM_002085.5:c.84+131_84+136del MANE Select NP_002076.2:n.84+131_84+136del