Canonical Allele Identifier: CA2576545183

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106616_1106617del , CM000681.2:g.1106616_1106617del	GRCh38
NC_000019.9:g.1106615_1106616del , CM000681.1:g.1106615_1106616del	GRCh37
NC_000019.8:g.1057615_1057616del	NCBI36
NG_050621.1:g.7691_7692del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585362.7:c.*44_*45del	ENSP00000473614.3:n.*44_*45del
ENST00000593032.6:c.618_619del	ENSP00000465828.4:p.Gly207SerfsTer?
ENST00000706713.1:c.*44_*45del	ENSP00000516510.1:n.*44_*45del
ENST00000706714.1:c.618_619del	ENSP00000516511.1:p.Gly207SerfsTer?
ENST00000706715.1:c.*44_*45del	ENSP00000516512.1:n.*44_*45del
ENST00000354171.13:c.*44_*45del MANE Select	ENSP00000346103.7:n.*44_*45del
ENST00000589115.6:c.*70_*71del	ENSP00000466872.3:n.*70_*71del
ENST00000354171.12:c.*44_*45del	ENSP00000346103.7:n.*44_*45del
ENST00000585480.1:c.338_339del	ENSP00000467900.1:p.Leu113Ter
ENST00000588919.5:c.579_580del	ENSP00000464989.3:p.Gly194SerfsTer?
ENST00000589115.5:c.*70_*71del	ENSP00000466872.2:n.*70_*71del
ENST00000592940.2:n.1009_1010del
ENST00000611653.4:c.*44_*45del	ENSP00000483655.1:n.*44_*45del
ENST00000616066.4:c.*44_*45del	ENSP00000485000.1:n.*44_*45del
ENST00000622390.4:c.*44_*45del	ENSP00000477503.1:n.*44_*45del
NM_001039847.2:c.660_661del	NP_001034936.1:p.Gly221SerfsTer?
NM_001039848.2:c.*44_*45del	NP_001034937.1:n.*44_*45del
NM_002085.4:c.*44_*45del	NP_002076.2:n.*44_*45del
NM_001039848.3:c.*44_*45del	NP_001034937.1:n.*44_*45del
NM_001039847.3:c.660_661del	NP_001034936.1:p.Gly221SerfsTer?
NM_001039848.4:c.*44_*45del	NP_001034937.1:n.*44_*45del
NM_001367832.1:c.*44_*45del	NP_001354761.1:n.*44_*45del
NM_002085.5:c.*44_*45del MANE Select	NP_002076.2:n.*44_*45del