Canonical Allele Identifier: CA2588207737

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106126-T-TAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106126_1106127insAGA , CM000681.2:g.1106126_1106127insAGA	GRCh38
NC_000019.9:g.1106125_1106126insAGA , CM000681.1:g.1106125_1106126insAGA	GRCh37
NC_000019.8:g.1057125_1057126insAGA	NCBI36
NG_050621.1:g.7201_7202insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-116_588-115insAGA	ENSP00000473614.3:n.588-116_588-115insAGA
ENST00000593032.6:c.396-55_396-54insAGA	ENSP00000465828.4:n.396-55_396-54insAGA
ENST00000706713.1:c.471-116_471-115insAGA	ENSP00000516510.1:n.471-116_471-115insAGA
ENST00000706714.1:c.396-55_396-54insAGA	ENSP00000516511.1:n.396-55_396-54insAGA
ENST00000706715.1:c.93-116_93-115insAGA	ENSP00000516512.1:n.93-116_93-115insAGA
ENST00000354171.13:c.477-116_477-115insAGA MANE Select	ENSP00000346103.7:n.477-116_477-115insAGA
ENST00000589115.6:c.477-274_477-273insAGA	ENSP00000466872.3:n.477-274_477-273insAGA
ENST00000354171.12:c.477-116_477-115insAGA	ENSP00000346103.7:n.477-116_477-115insAGA
ENST00000585480.1:c.210-116_210-115insAGA	ENSP00000467900.1:n.210-116_210-115insAGA
ENST00000587648.5:c.357-116_357-115insAGA	ENSP00000468349.1:n.357-116_357-115insAGA
ENST00000588919.5:c.396-116_396-115insAGA	ENSP00000464989.3:n.396-116_396-115insAGA
ENST00000589115.5:c.477-274_477-273insAGA	ENSP00000466872.2:n.477-274_477-273insAGA
ENST00000592940.2:n.732_733insAGA
ENST00000593032.5:c.396-55_396-54insAGA	ENSP00000465828.3:n.396-55_396-54insAGA
ENST00000611653.4:c.396-116_396-115insAGA	ENSP00000483655.1:n.396-116_396-115insAGA
ENST00000616066.4:c.474-116_474-115insAGA	ENSP00000485000.1:n.474-116_474-115insAGA
ENST00000622390.4:c.585-116_585-115insAGA	ENSP00000477503.1:n.585-116_585-115insAGA
NM_001039847.2:c.477-116_477-115insAGA	NP_001034936.1:n.477-116_477-115insAGA
NM_001039848.2:c.588-116_588-115insAGA	NP_001034937.1:n.588-116_588-115insAGA
NM_002085.4:c.477-116_477-115insAGA	NP_002076.2:n.477-116_477-115insAGA
NM_001039848.3:c.588-116_588-115insAGA	NP_001034937.1:n.588-116_588-115insAGA
NM_001039847.3:c.477-116_477-115insAGA	NP_001034936.1:n.477-116_477-115insAGA
NM_001039848.4:c.588-116_588-115insAGA	NP_001034937.1:n.588-116_588-115insAGA
NM_001367832.1:c.396-116_396-115insAGA	NP_001354761.1:n.396-116_396-115insAGA
NM_002085.5:c.477-116_477-115insAGA MANE Select	NP_002076.2:n.477-116_477-115insAGA