Canonical Allele Identifier: CA2317520377

Gene: GPX4

Linked Data

• dbSNP Id: rs2079649533
• gnomAD v4: 19-1106069-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106073_1106074del , CM000681.2:g.1106073_1106074del	GRCh38
NC_000019.9:g.1106072_1106073del , CM000681.1:g.1106072_1106073del	GRCh37
NC_000019.8:g.1057072_1057073del	NCBI36
NG_050621.1:g.7148_7149del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-169_588-168del	ENSP00000473614.3:n.588-169_588-168del
ENST00000593032.6:c.396-108_396-107del	ENSP00000465828.4:n.396-108_396-107del
ENST00000706713.1:c.471-169_471-168del	ENSP00000516510.1:n.471-169_471-168del
ENST00000706714.1:c.396-108_396-107del	ENSP00000516511.1:n.396-108_396-107del
ENST00000706715.1:c.93-169_93-168del	ENSP00000516512.1:n.93-169_93-168del
ENST00000354171.13:c.477-169_477-168del MANE Select	ENSP00000346103.7:n.477-169_477-168del
ENST00000589115.6:c.476+264_476+265del	ENSP00000466872.3:n.476+264_476+265del
ENST00000354171.12:c.477-169_477-168del	ENSP00000346103.7:n.477-169_477-168del
ENST00000585480.1:c.210-169_210-168del	ENSP00000467900.1:n.210-169_210-168del
ENST00000587648.5:c.357-169_357-168del	ENSP00000468349.1:n.357-169_357-168del
ENST00000588919.5:c.396-169_396-168del	ENSP00000464989.3:n.396-169_396-168del
ENST00000589115.5:c.476+264_476+265del	ENSP00000466872.2:n.476+264_476+265del
ENST00000592940.2:n.679_680del
ENST00000593032.5:c.396-108_396-107del	ENSP00000465828.3:n.396-108_396-107del
ENST00000611653.4:c.396-169_396-168del	ENSP00000483655.1:n.396-169_396-168del
ENST00000616066.4:c.474-169_474-168del	ENSP00000485000.1:n.474-169_474-168del
ENST00000622390.4:c.585-169_585-168del	ENSP00000477503.1:n.585-169_585-168del
NM_001039847.2:c.477-169_477-168del	NP_001034936.1:n.477-169_477-168del
NM_001039848.2:c.588-169_588-168del	NP_001034937.1:n.588-169_588-168del
NM_002085.4:c.477-169_477-168del	NP_002076.2:n.477-169_477-168del
NM_001039848.3:c.588-169_588-168del	NP_001034937.1:n.588-169_588-168del
NM_001039847.3:c.477-169_477-168del	NP_001034936.1:n.477-169_477-168del
NM_001039848.4:c.588-169_588-168del	NP_001034937.1:n.588-169_588-168del
NM_001367832.1:c.396-169_396-168del	NP_001354761.1:n.396-169_396-168del
NM_002085.5:c.477-169_477-168del MANE Select	NP_002076.2:n.477-169_477-168del