Canonical Allele Identifier: CA2317520242

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105904_1105905delinsCG , CM000681.2:g.1105904_1105905delinsCG	GRCh38
NC_000019.9:g.1105903_1105904delinsCG , CM000681.1:g.1105903_1105904delinsCG	GRCh37
NC_000019.8:g.1056903_1056904delinsCG	NCBI36
NG_050621.1:g.6979_6980delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.587+95_587+96delinsCG	ENSP00000473614.3:n.587+95_587+96delinsCG
ENST00000593032.6:c.395+95_395+96delinsCG	ENSP00000465828.4:n.395+95_395+96delinsCG
ENST00000706713.1:c.470+95_470+96delinsCG	ENSP00000516510.1:n.470+95_470+96delinsCG
ENST00000706714.1:c.395+95_395+96delinsCG	ENSP00000516511.1:n.395+95_395+96delinsCG
ENST00000706715.1:c.92+95_92+96delinsCG	ENSP00000516512.1:n.92+95_92+96delinsCG
ENST00000354171.13:c.476+95_476+96delinsCG MANE Select	ENSP00000346103.7:n.476+95_476+96delinsCG
ENST00000589115.6:c.476+95_476+96delinsCG	ENSP00000466872.3:n.476+95_476+96delinsCG
ENST00000354171.12:c.476+95_476+96delinsCG	ENSP00000346103.7:n.476+95_476+96delinsCG
ENST00000585480.1:c.209+95_209+96delinsCG	ENSP00000467900.1:n.209+95_209+96delinsCG
ENST00000587648.5:c.356+95_356+96delinsCG	ENSP00000468349.1:n.356+95_356+96delinsCG
ENST00000588919.5:c.395+95_395+96delinsCG	ENSP00000464989.3:n.395+95_395+96delinsCG
ENST00000589115.5:c.476+95_476+96delinsCG	ENSP00000466872.2:n.476+95_476+96delinsCG
ENST00000592940.2:n.510_511delinsCG
ENST00000593032.5:c.395+95_395+96delinsCG	ENSP00000465828.3:n.395+95_395+96delinsCG
ENST00000611653.4:c.395+95_395+96delinsCG	ENSP00000483655.1:n.395+95_395+96delinsCG
ENST00000616066.4:c.473+95_473+96delinsCG	ENSP00000485000.1:n.473+95_473+96delinsCG
ENST00000622390.4:c.584+95_584+96delinsCG	ENSP00000477503.1:n.584+95_584+96delinsCG
NM_001039847.2:c.476+95_476+96delinsCG	NP_001034936.1:n.476+95_476+96delinsCG
NM_001039848.2:c.587+95_587+96delinsCG	NP_001034937.1:n.587+95_587+96delinsCG
NM_002085.4:c.476+95_476+96delinsCG	NP_002076.2:n.476+95_476+96delinsCG
NM_001039848.3:c.587+95_587+96delinsCG	NP_001034937.1:n.587+95_587+96delinsCG
NM_001039847.3:c.476+95_476+96delinsCG	NP_001034936.1:n.476+95_476+96delinsCG
NM_001039848.4:c.587+95_587+96delinsCG	NP_001034937.1:n.587+95_587+96delinsCG
NM_001367832.1:c.395+95_395+96delinsCG	NP_001354761.1:n.395+95_395+96delinsCG
NM_002085.5:c.476+95_476+96delinsCG MANE Select	NP_002076.2:n.476+95_476+96delinsCG