Canonical Allele Identifier: CA2741604411

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105858_1105859insGGGGGGGGGGGGGG , CM000681.2:g.1105858_1105859insGGGGGGGGGGGGGG	GRCh38
NC_000019.9:g.1105857_1105858insGGGGGGGGGGGGGG , CM000681.1:g.1105857_1105858insGGGGGGGGGGGGGG	GRCh37
NC_000019.8:g.1056857_1056858insGGGGGGGGGGGGGG	NCBI36
NG_050621.1:g.6933_6934insGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.587+49_587+50insGGGGGGGGGGGGGG	ENSP00000473614.3:n.587+49_587+50insGGGGGGGGGGGGGG
ENST00000593032.6:c.395+49_395+50insGGGGGGGGGGGGGG	ENSP00000465828.4:n.395+49_395+50insGGGGGGGGGGGGGG
ENST00000706713.1:c.470+49_470+50insGGGGGGGGGGGGGG	ENSP00000516510.1:n.470+49_470+50insGGGGGGGGGGGGGG
ENST00000706714.1:c.395+49_395+50insGGGGGGGGGGGGGG	ENSP00000516511.1:n.395+49_395+50insGGGGGGGGGGGGGG
ENST00000706715.1:c.92+49_92+50insGGGGGGGGGGGGGG	ENSP00000516512.1:n.92+49_92+50insGGGGGGGGGGGGGG
ENST00000354171.13:c.476+49_476+50insGGGGGGGGGGGGGG MANE Select	ENSP00000346103.7:n.476+49_476+50insGGGGGGGGGGGGGG
ENST00000589115.6:c.476+49_476+50insGGGGGGGGGGGGGG	ENSP00000466872.3:n.476+49_476+50insGGGGGGGGGGGGGG
ENST00000354171.12:c.476+49_476+50insGGGGGGGGGGGGGG	ENSP00000346103.7:n.476+49_476+50insGGGGGGGGGGGGGG
ENST00000585480.1:c.209+49_209+50insGGGGGGGGGGGGGG	ENSP00000467900.1:n.209+49_209+50insGGGGGGGGGGGGGG
ENST00000587648.5:c.356+49_356+50insGGGGGGGGGGGGGG	ENSP00000468349.1:n.356+49_356+50insGGGGGGGGGGGGGG
ENST00000588919.5:c.395+49_395+50insGGGGGGGGGGGGGG	ENSP00000464989.3:n.395+49_395+50insGGGGGGGGGGGGGG
ENST00000589115.5:c.476+49_476+50insGGGGGGGGGGGGGG	ENSP00000466872.2:n.476+49_476+50insGGGGGGGGGGGGGG
ENST00000592940.2:n.464_465insGGGGGGGGGGGGGG
ENST00000593032.5:c.395+49_395+50insGGGGGGGGGGGGGG	ENSP00000465828.3:n.395+49_395+50insGGGGGGGGGGGGGG
ENST00000611653.4:c.395+49_395+50insGGGGGGGGGGGGGG	ENSP00000483655.1:n.395+49_395+50insGGGGGGGGGGGGGG
ENST00000616066.4:c.473+49_473+50insGGGGGGGGGGGGGG	ENSP00000485000.1:n.473+49_473+50insGGGGGGGGGGGGGG
ENST00000622390.4:c.584+49_584+50insGGGGGGGGGGGGGG	ENSP00000477503.1:n.584+49_584+50insGGGGGGGGGGGGGG
NM_001039847.2:c.476+49_476+50insGGGGGGGGGGGGGG	NP_001034936.1:n.476+49_476+50insGGGGGGGGGGGGGG
NM_001039848.2:c.587+49_587+50insGGGGGGGGGGGGGG	NP_001034937.1:n.587+49_587+50insGGGGGGGGGGGGGG
NM_002085.4:c.476+49_476+50insGGGGGGGGGGGGGG	NP_002076.2:n.476+49_476+50insGGGGGGGGGGGGGG
NM_001039848.3:c.587+49_587+50insGGGGGGGGGGGGGG	NP_001034937.1:n.587+49_587+50insGGGGGGGGGGGGGG
NM_001039847.3:c.476+49_476+50insGGGGGGGGGGGGGG	NP_001034936.1:n.476+49_476+50insGGGGGGGGGGGGGG
NM_001039848.4:c.587+49_587+50insGGGGGGGGGGGGGG	NP_001034937.1:n.587+49_587+50insGGGGGGGGGGGGGG
NM_001367832.1:c.395+49_395+50insGGGGGGGGGGGGGG	NP_001354761.1:n.395+49_395+50insGGGGGGGGGGGGGG
NM_002085.5:c.476+49_476+50insGGGGGGGGGGGGGG MANE Select	NP_002076.2:n.476+49_476+50insGGGGGGGGGGGGGG