Canonical Allele Identifier: CA2588207896

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106616-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106616_1106617insC , CM000681.2:g.1106616_1106617insC	GRCh38
NC_000019.9:g.1106615_1106616insC , CM000681.1:g.1106615_1106616insC	GRCh37
NC_000019.8:g.1057615_1057616insC	NCBI36
NG_050621.1:g.7691_7692insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.*44_*45insC	ENSP00000473614.3:n.*44_*45insC
ENST00000593032.6:c.618_619insC	ENSP00000465828.4:p.Gly207ArgfsTer?
ENST00000706713.1:c.*44_*45insC	ENSP00000516510.1:n.*44_*45insC
ENST00000706714.1:c.618_619insC	ENSP00000516511.1:p.Gly207ArgfsTer?
ENST00000706715.1:c.*44_*45insC	ENSP00000516512.1:n.*44_*45insC
ENST00000354171.13:c.*44_*45insC MANE Select	ENSP00000346103.7:n.*44_*45insC
ENST00000589115.6:c.*70_*71insC	ENSP00000466872.3:n.*70_*71insC
ENST00000354171.12:c.*44_*45insC	ENSP00000346103.7:n.*44_*45insC
ENST00000585480.1:c.338_339insC	ENSP00000467900.1:p.Leu113PhefsTer9
ENST00000588919.5:c.579_580insC	ENSP00000464989.3:p.Gly194ArgfsTer?
ENST00000589115.5:c.*70_*71insC	ENSP00000466872.2:n.*70_*71insC
ENST00000592940.2:n.1009_1010insC
ENST00000611653.4:c.*44_*45insC	ENSP00000483655.1:n.*44_*45insC
ENST00000616066.4:c.*44_*45insC	ENSP00000485000.1:n.*44_*45insC
ENST00000622390.4:c.*44_*45insC	ENSP00000477503.1:n.*44_*45insC
NM_001039847.2:c.660_661insC	NP_001034936.1:p.Gly221ArgfsTer?
NM_001039848.2:c.*44_*45insC	NP_001034937.1:n.*44_*45insC
NM_002085.4:c.*44_*45insC	NP_002076.2:n.*44_*45insC
NM_001039848.3:c.*44_*45insC	NP_001034937.1:n.*44_*45insC
NM_001039847.3:c.660_661insC	NP_001034936.1:p.Gly221ArgfsTer?
NM_001039848.4:c.*44_*45insC	NP_001034937.1:n.*44_*45insC
NM_001367832.1:c.*44_*45insC	NP_001354761.1:n.*44_*45insC
NM_002085.5:c.*44_*45insC MANE Select	NP_002076.2:n.*44_*45insC