Canonical Allele Identifier: CA2317519068

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104095_1104096delinsGC , CM000681.2:g.1104095_1104096delinsGC	GRCh38
NC_000019.9:g.1104094_1104095delinsGC , CM000681.1:g.1104094_1104095delinsGC	GRCh37
NC_000019.8:g.1055094_1055095delinsGC	NCBI36
NG_050621.1:g.5170_5171delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000593032.6:c.-30_-29delinsGC	ENSP00000465828.4:n.-30_-29delinsGC
ENST00000706713.1:c.52_53delinsGC	ENSP00000516510.1:p.Ala18=
ENST00000706714.1:c.-30_-29delinsGC	ENSP00000516511.1:n.-30_-29delinsGC
ENST00000354171.13:c.52_53delinsGC MANE Select	ENSP00000346103.7:p.Ala18=
ENST00000589115.6:c.52_53delinsGC	ENSP00000466872.3:p.Ala18=
ENST00000354171.12:c.52_53delinsGC	ENSP00000346103.7:p.Ala18=
ENST00000588919.5:c.-30_-29delinsGC	ENSP00000464989.3:n.-30_-29delinsGC
ENST00000589115.5:c.52_53delinsGC	ENSP00000466872.2:p.Ala18=
ENST00000593032.5:c.-30_-29delinsGC	ENSP00000465828.3:n.-30_-29delinsGC
ENST00000611653.4:c.-30_-29delinsGC	ENSP00000483655.1:n.-30_-29delinsGC
ENST00000616066.4:c.52_53delinsGC	ENSP00000485000.1:p.Ala18=
NM_001039847.2:c.52_53delinsGC	NP_001034936.1:p.Ala18=
NM_002085.4:c.52_53delinsGC	NP_002076.2:p.Ala18=
NM_001039847.3:c.52_53delinsGC	NP_001034936.1:p.Ala18=
NM_001367832.1:c.-30_-29delinsGC	NP_001354761.1:n.-30_-29delinsGC
NM_002085.5:c.52_53delinsGC MANE Select	NP_002076.2:p.Ala18=