Canonical Allele Identifier: CA9037373

Gene: GPX4

Linked Data

• dbSNP Id: rs777951433
• ExAC: 19:1105832 CGGCTGCTGGGGTGGGGGTGGGGG / C
• gnomAD v2: 19-1105832-CGGCTGCTGGGGTGGGGGTGGGGG-C
• gnomAD v3: 19-1105833-CGGCTGCTGGGGTGGGGGTGGGGG-C
• gnomAD v4: 19-1105833-CGGCTGCTGGGGTGGGGGTGGGGG-C
• MyVariant Identifiers: chr19:g.1105833_1105855del (hg19) ; chr19:g.1105834_1105856del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105844_1105866del , CM000681.2:g.1105844_1105866del	GRCh38
NC_000019.9:g.1105843_1105865del , CM000681.1:g.1105843_1105865del	GRCh37
NC_000019.8:g.1056843_1056865del	NCBI36
NG_050621.1:g.6919_6941del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.587+35_587+57del	ENSP00000473614.3:n.587+35_587+57del
ENST00000593032.6:c.395+35_395+57del	ENSP00000465828.4:n.395+35_395+57del
ENST00000706713.1:c.470+35_470+57del	ENSP00000516510.1:n.470+35_470+57del
ENST00000706714.1:c.395+35_395+57del	ENSP00000516511.1:n.395+35_395+57del
ENST00000706715.1:c.92+35_92+57del	ENSP00000516512.1:n.92+35_92+57del
ENST00000354171.13:c.476+35_476+57del MANE Select	ENSP00000346103.7:n.476+35_476+57del
ENST00000589115.6:c.476+35_476+57del	ENSP00000466872.3:n.476+35_476+57del
ENST00000354171.12:c.476+35_476+57del	ENSP00000346103.7:n.476+35_476+57del
ENST00000585480.1:c.209+35_209+57del	ENSP00000467900.1:n.209+35_209+57del
ENST00000587648.5:c.356+35_356+57del	ENSP00000468349.1:n.356+35_356+57del
ENST00000588919.5:c.395+35_395+57del	ENSP00000464989.3:n.395+35_395+57del
ENST00000589115.5:c.476+35_476+57del	ENSP00000466872.2:n.476+35_476+57del
ENST00000592940.2:n.450_472del
ENST00000593032.5:c.395+35_395+57del	ENSP00000465828.3:n.395+35_395+57del
ENST00000611653.4:c.395+35_395+57del	ENSP00000483655.1:n.395+35_395+57del
ENST00000616066.4:c.473+35_473+57del	ENSP00000485000.1:n.473+35_473+57del
ENST00000622390.4:c.584+35_584+57del	ENSP00000477503.1:n.584+35_584+57del
NM_001039847.2:c.476+35_476+57del	NP_001034936.1:n.476+35_476+57del
NM_001039848.2:c.587+35_587+57del	NP_001034937.1:n.587+35_587+57del
NM_002085.4:c.476+35_476+57del	NP_002076.2:n.476+35_476+57del
NM_001039848.3:c.587+35_587+57del	NP_001034937.1:n.587+35_587+57del
NM_001039847.3:c.476+35_476+57del	NP_001034936.1:n.476+35_476+57del
NM_001039848.4:c.587+35_587+57del	NP_001034937.1:n.587+35_587+57del
NM_001367832.1:c.395+35_395+57del	NP_001354761.1:n.395+35_395+57del
NM_002085.5:c.476+35_476+57del MANE Select	NP_002076.2:n.476+35_476+57del