Canonical Allele Identifier: CA2588207352

Gene: GPX4

Linked Data

• gnomAD v4: 19-1105914-T-TGCTGGCTGCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105914_1105915insGCTGGCTGCAG , CM000681.2:g.1105914_1105915insGCTGGCTGCAG	GRCh38
NC_000019.9:g.1105913_1105914insGCTGGCTGCAG , CM000681.1:g.1105913_1105914insGCTGGCTGCAG	GRCh37
NC_000019.8:g.1056913_1056914insGCTGGCTGCAG	NCBI36
NG_050621.1:g.6989_6990insGCTGGCTGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.587+105_587+106insGCTGGCTGCAG	ENSP00000473614.3:n.587+105_587+106insGCTGGCTGCAG
ENST00000593032.6:c.395+105_395+106insGCTGGCTGCAG	ENSP00000465828.4:n.395+105_395+106insGCTGGCTGCAG
ENST00000706713.1:c.470+105_470+106insGCTGGCTGCAG	ENSP00000516510.1:n.470+105_470+106insGCTGGCTGCAG
ENST00000706714.1:c.395+105_395+106insGCTGGCTGCAG	ENSP00000516511.1:n.395+105_395+106insGCTGGCTGCAG
ENST00000706715.1:c.92+105_92+106insGCTGGCTGCAG	ENSP00000516512.1:n.92+105_92+106insGCTGGCTGCAG
ENST00000354171.13:c.476+105_476+106insGCTGGCTGCAG MANE Select	ENSP00000346103.7:n.476+105_476+106insGCTGGCTGCAG
ENST00000589115.6:c.476+105_476+106insGCTGGCTGCAG	ENSP00000466872.3:n.476+105_476+106insGCTGGCTGCAG
ENST00000354171.12:c.476+105_476+106insGCTGGCTGCAG	ENSP00000346103.7:n.476+105_476+106insGCTGGCTGCAG
ENST00000585480.1:c.209+105_209+106insGCTGGCTGCAG	ENSP00000467900.1:n.209+105_209+106insGCTGGCTGCAG
ENST00000587648.5:c.356+105_356+106insGCTGGCTGCAG	ENSP00000468349.1:n.356+105_356+106insGCTGGCTGCAG
ENST00000588919.5:c.395+105_395+106insGCTGGCTGCAG	ENSP00000464989.3:n.395+105_395+106insGCTGGCTGCAG
ENST00000589115.5:c.476+105_476+106insGCTGGCTGCAG	ENSP00000466872.2:n.476+105_476+106insGCTGGCTGCAG
ENST00000592940.2:n.520_521insGCTGGCTGCAG
ENST00000593032.5:c.395+105_395+106insGCTGGCTGCAG	ENSP00000465828.3:n.395+105_395+106insGCTGGCTGCAG
ENST00000611653.4:c.395+105_395+106insGCTGGCTGCAG	ENSP00000483655.1:n.395+105_395+106insGCTGGCTGCAG
ENST00000616066.4:c.473+105_473+106insGCTGGCTGCAG	ENSP00000485000.1:n.473+105_473+106insGCTGGCTGCAG
ENST00000622390.4:c.584+105_584+106insGCTGGCTGCAG	ENSP00000477503.1:n.584+105_584+106insGCTGGCTGCAG
NM_001039847.2:c.476+105_476+106insGCTGGCTGCAG	NP_001034936.1:n.476+105_476+106insGCTGGCTGCAG
NM_001039848.2:c.587+105_587+106insGCTGGCTGCAG	NP_001034937.1:n.587+105_587+106insGCTGGCTGCAG
NM_002085.4:c.476+105_476+106insGCTGGCTGCAG	NP_002076.2:n.476+105_476+106insGCTGGCTGCAG
NM_001039848.3:c.587+105_587+106insGCTGGCTGCAG	NP_001034937.1:n.587+105_587+106insGCTGGCTGCAG
NM_001039847.3:c.476+105_476+106insGCTGGCTGCAG	NP_001034936.1:n.476+105_476+106insGCTGGCTGCAG
NM_001039848.4:c.587+105_587+106insGCTGGCTGCAG	NP_001034937.1:n.587+105_587+106insGCTGGCTGCAG
NM_001367832.1:c.395+105_395+106insGCTGGCTGCAG	NP_001354761.1:n.395+105_395+106insGCTGGCTGCAG
NM_002085.5:c.476+105_476+106insGCTGGCTGCAG MANE Select	NP_002076.2:n.476+105_476+106insGCTGGCTGCAG