Canonical Allele Identifier: CA2588207346

Gene: GPX4

Linked Data

• gnomAD v4: 19-1105911-C-CTGTGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105911_1105912insTGTGCT , CM000681.2:g.1105911_1105912insTGTGCT	GRCh38
NC_000019.9:g.1105910_1105911insTGTGCT , CM000681.1:g.1105910_1105911insTGTGCT	GRCh37
NC_000019.8:g.1056910_1056911insTGTGCT	NCBI36
NG_050621.1:g.6986_6987insTGTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.587+102_587+103insTGTGCT	ENSP00000473614.3:n.587+102_587+103insTGTGCT
ENST00000593032.6:c.395+102_395+103insTGTGCT	ENSP00000465828.4:n.395+102_395+103insTGTGCT
ENST00000706713.1:c.470+102_470+103insTGTGCT	ENSP00000516510.1:n.470+102_470+103insTGTGCT
ENST00000706714.1:c.395+102_395+103insTGTGCT	ENSP00000516511.1:n.395+102_395+103insTGTGCT
ENST00000706715.1:c.92+102_92+103insTGTGCT	ENSP00000516512.1:n.92+102_92+103insTGTGCT
ENST00000354171.13:c.476+102_476+103insTGTGCT MANE Select	ENSP00000346103.7:n.476+102_476+103insTGTGCT
ENST00000589115.6:c.476+102_476+103insTGTGCT	ENSP00000466872.3:n.476+102_476+103insTGTGCT
ENST00000354171.12:c.476+102_476+103insTGTGCT	ENSP00000346103.7:n.476+102_476+103insTGTGCT
ENST00000585480.1:c.209+102_209+103insTGTGCT	ENSP00000467900.1:n.209+102_209+103insTGTGCT
ENST00000587648.5:c.356+102_356+103insTGTGCT	ENSP00000468349.1:n.356+102_356+103insTGTGCT
ENST00000588919.5:c.395+102_395+103insTGTGCT	ENSP00000464989.3:n.395+102_395+103insTGTGCT
ENST00000589115.5:c.476+102_476+103insTGTGCT	ENSP00000466872.2:n.476+102_476+103insTGTGCT
ENST00000592940.2:n.517_518insTGTGCT
ENST00000593032.5:c.395+102_395+103insTGTGCT	ENSP00000465828.3:n.395+102_395+103insTGTGCT
ENST00000611653.4:c.395+102_395+103insTGTGCT	ENSP00000483655.1:n.395+102_395+103insTGTGCT
ENST00000616066.4:c.473+102_473+103insTGTGCT	ENSP00000485000.1:n.473+102_473+103insTGTGCT
ENST00000622390.4:c.584+102_584+103insTGTGCT	ENSP00000477503.1:n.584+102_584+103insTGTGCT
NM_001039847.2:c.476+102_476+103insTGTGCT	NP_001034936.1:n.476+102_476+103insTGTGCT
NM_001039848.2:c.587+102_587+103insTGTGCT	NP_001034937.1:n.587+102_587+103insTGTGCT
NM_002085.4:c.476+102_476+103insTGTGCT	NP_002076.2:n.476+102_476+103insTGTGCT
NM_001039848.3:c.587+102_587+103insTGTGCT	NP_001034937.1:n.587+102_587+103insTGTGCT
NM_001039847.3:c.476+102_476+103insTGTGCT	NP_001034936.1:n.476+102_476+103insTGTGCT
NM_001039848.4:c.587+102_587+103insTGTGCT	NP_001034937.1:n.587+102_587+103insTGTGCT
NM_001367832.1:c.395+102_395+103insTGTGCT	NP_001354761.1:n.395+102_395+103insTGTGCT
NM_002085.5:c.476+102_476+103insTGTGCT MANE Select	NP_002076.2:n.476+102_476+103insTGTGCT