Canonical Allele Identifier: CA2588207658

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106079-TGCATG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106082_1106086del , CM000681.2:g.1106082_1106086del	GRCh38
NC_000019.9:g.1106081_1106085del , CM000681.1:g.1106081_1106085del	GRCh37
NC_000019.8:g.1057081_1057085del	NCBI36
NG_050621.1:g.7157_7161del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-160_588-156del	ENSP00000473614.3:n.588-160_588-156del
ENST00000593032.6:c.396-99_396-95del	ENSP00000465828.4:n.396-99_396-95del
ENST00000706713.1:c.471-160_471-156del	ENSP00000516510.1:n.471-160_471-156del
ENST00000706714.1:c.396-99_396-95del	ENSP00000516511.1:n.396-99_396-95del
ENST00000706715.1:c.93-160_93-156del	ENSP00000516512.1:n.93-160_93-156del
ENST00000354171.13:c.477-160_477-156del MANE Select	ENSP00000346103.7:n.477-160_477-156del
ENST00000589115.6:c.476+273_476+277del	ENSP00000466872.3:n.476+273_476+277del
ENST00000354171.12:c.477-160_477-156del	ENSP00000346103.7:n.477-160_477-156del
ENST00000585480.1:c.210-160_210-156del	ENSP00000467900.1:n.210-160_210-156del
ENST00000587648.5:c.357-160_357-156del	ENSP00000468349.1:n.357-160_357-156del
ENST00000588919.5:c.396-160_396-156del	ENSP00000464989.3:n.396-160_396-156del
ENST00000589115.5:c.476+273_476+277del	ENSP00000466872.2:n.476+273_476+277del
ENST00000592940.2:n.688_692del
ENST00000593032.5:c.396-99_396-95del	ENSP00000465828.3:n.396-99_396-95del
ENST00000611653.4:c.396-160_396-156del	ENSP00000483655.1:n.396-160_396-156del
ENST00000616066.4:c.474-160_474-156del	ENSP00000485000.1:n.474-160_474-156del
ENST00000622390.4:c.585-160_585-156del	ENSP00000477503.1:n.585-160_585-156del
NM_001039847.2:c.477-160_477-156del	NP_001034936.1:n.477-160_477-156del
NM_001039848.2:c.588-160_588-156del	NP_001034937.1:n.588-160_588-156del
NM_002085.4:c.477-160_477-156del	NP_002076.2:n.477-160_477-156del
NM_001039848.3:c.588-160_588-156del	NP_001034937.1:n.588-160_588-156del
NM_001039847.3:c.477-160_477-156del	NP_001034936.1:n.477-160_477-156del
NM_001039848.4:c.588-160_588-156del	NP_001034937.1:n.588-160_588-156del
NM_001367832.1:c.396-160_396-156del	NP_001354761.1:n.396-160_396-156del
NM_002085.5:c.477-160_477-156del MANE Select	NP_002076.2:n.477-160_477-156del