Canonical Allele Identifier: CA9037379

Gene: GPX4

Linked Data

• dbSNP Id: rs762541815
• ExAC: 19:1105850 T / TGGGGGG
• MyVariant Identifiers: chr19:g.1105852_1105853insGGGGGG (hg19) ; chr19:g.1105850_1105851insGGGGGG (hg19) ; chr19:g.1105851_1105852insGGGGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105853_1105858dup , CM000681.2:g.1105853_1105858dup	GRCh38
NC_000019.9:g.1105852_1105857dup , CM000681.1:g.1105852_1105857dup	GRCh37
NC_000019.8:g.1056852_1056857dup	NCBI36
NG_050621.1:g.6928_6933dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.587+44_587+49dup	ENSP00000473614.3:n.587+44_587+49dup
ENST00000593032.6:c.395+44_395+49dup	ENSP00000465828.4:n.395+44_395+49dup
ENST00000706713.1:c.470+44_470+49dup	ENSP00000516510.1:n.470+44_470+49dup
ENST00000706714.1:c.395+44_395+49dup	ENSP00000516511.1:n.395+44_395+49dup
ENST00000706715.1:c.92+44_92+49dup	ENSP00000516512.1:n.92+44_92+49dup
ENST00000354171.13:c.476+44_476+49dup MANE Select	ENSP00000346103.7:n.476+44_476+49dup
ENST00000589115.6:c.476+44_476+49dup	ENSP00000466872.3:n.476+44_476+49dup
ENST00000354171.12:c.476+44_476+49dup	ENSP00000346103.7:n.476+44_476+49dup
ENST00000585480.1:c.209+44_209+49dup	ENSP00000467900.1:n.209+44_209+49dup
ENST00000587648.5:c.356+44_356+49dup	ENSP00000468349.1:n.356+44_356+49dup
ENST00000588919.5:c.395+44_395+49dup	ENSP00000464989.3:n.395+44_395+49dup
ENST00000589115.5:c.476+44_476+49dup	ENSP00000466872.2:n.476+44_476+49dup
ENST00000592940.2:n.459_464dup
ENST00000593032.5:c.395+44_395+49dup	ENSP00000465828.3:n.395+44_395+49dup
ENST00000611653.4:c.395+44_395+49dup	ENSP00000483655.1:n.395+44_395+49dup
ENST00000616066.4:c.473+44_473+49dup	ENSP00000485000.1:n.473+44_473+49dup
ENST00000622390.4:c.584+44_584+49dup	ENSP00000477503.1:n.584+44_584+49dup
NM_001039847.2:c.476+44_476+49dup	NP_001034936.1:n.476+44_476+49dup
NM_001039848.2:c.587+44_587+49dup	NP_001034937.1:n.587+44_587+49dup
NM_002085.4:c.476+44_476+49dup	NP_002076.2:n.476+44_476+49dup
NM_001039848.3:c.587+44_587+49dup	NP_001034937.1:n.587+44_587+49dup
NM_001039847.3:c.476+44_476+49dup	NP_001034936.1:n.476+44_476+49dup
NM_001039848.4:c.587+44_587+49dup	NP_001034937.1:n.587+44_587+49dup
NM_001367832.1:c.395+44_395+49dup	NP_001354761.1:n.395+44_395+49dup
NM_002085.5:c.476+44_476+49dup MANE Select	NP_002076.2:n.476+44_476+49dup