Canonical Allele Identifier: CA2588207717

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106117-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106121_1106122dup , CM000681.2:g.1106121_1106122dup	GRCh38
NC_000019.9:g.1106120_1106121dup , CM000681.1:g.1106120_1106121dup	GRCh37
NC_000019.8:g.1057120_1057121dup	NCBI36
NG_050621.1:g.7196_7197dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-121_588-120dup	ENSP00000473614.3:n.588-121_588-120dup
ENST00000593032.6:c.396-60_396-59dup	ENSP00000465828.4:n.396-60_396-59dup
ENST00000706713.1:c.471-121_471-120dup	ENSP00000516510.1:n.471-121_471-120dup
ENST00000706714.1:c.396-60_396-59dup	ENSP00000516511.1:n.396-60_396-59dup
ENST00000706715.1:c.93-121_93-120dup	ENSP00000516512.1:n.93-121_93-120dup
ENST00000354171.13:c.477-121_477-120dup MANE Select	ENSP00000346103.7:n.477-121_477-120dup
ENST00000589115.6:c.477-279_477-278dup	ENSP00000466872.3:n.477-279_477-278dup
ENST00000354171.12:c.477-121_477-120dup	ENSP00000346103.7:n.477-121_477-120dup
ENST00000585480.1:c.210-121_210-120dup	ENSP00000467900.1:n.210-121_210-120dup
ENST00000587648.5:c.357-121_357-120dup	ENSP00000468349.1:n.357-121_357-120dup
ENST00000588919.5:c.396-121_396-120dup	ENSP00000464989.3:n.396-121_396-120dup
ENST00000589115.5:c.477-279_477-278dup	ENSP00000466872.2:n.477-279_477-278dup
ENST00000592940.2:n.727_728dup
ENST00000593032.5:c.396-60_396-59dup	ENSP00000465828.3:n.396-60_396-59dup
ENST00000611653.4:c.396-121_396-120dup	ENSP00000483655.1:n.396-121_396-120dup
ENST00000616066.4:c.474-121_474-120dup	ENSP00000485000.1:n.474-121_474-120dup
ENST00000622390.4:c.585-121_585-120dup	ENSP00000477503.1:n.585-121_585-120dup
NM_001039847.2:c.477-121_477-120dup	NP_001034936.1:n.477-121_477-120dup
NM_001039848.2:c.588-121_588-120dup	NP_001034937.1:n.588-121_588-120dup
NM_002085.4:c.477-121_477-120dup	NP_002076.2:n.477-121_477-120dup
NM_001039848.3:c.588-121_588-120dup	NP_001034937.1:n.588-121_588-120dup
NM_001039847.3:c.477-121_477-120dup	NP_001034936.1:n.477-121_477-120dup
NM_001039848.4:c.588-121_588-120dup	NP_001034937.1:n.588-121_588-120dup
NM_001367832.1:c.396-121_396-120dup	NP_001354761.1:n.396-121_396-120dup
NM_002085.5:c.477-121_477-120dup MANE Select	NP_002076.2:n.477-121_477-120dup