Canonical Allele Identifier: CA2813238551

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106430_1106431insCGCGTGA , CM000681.2:g.1106430_1106431insCGCGTGA	GRCh38
NC_000019.9:g.1106429_1106430insCGCGTGA , CM000681.1:g.1106429_1106430insCGCGTGA	GRCh37
NC_000019.8:g.1057429_1057430insCGCGTGA	NCBI36
NG_050621.1:g.7505_7506insCGCGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.643_644insCGCGTGA	ENSP00000473614.3:p.Lys215ThrfsTer?
ENST00000593032.6:c.512_513insCGCGTGA	ENSP00000465828.4:p.Glu171AspfsTer3
ENST00000706713.1:c.526_527insCGCGTGA	ENSP00000516510.1:p.Lys176ThrfsTer?
ENST00000706714.1:c.512_513insCGCGTGA	ENSP00000516511.1:p.Glu171AspfsTer3
ENST00000706715.1:c.148_149insCGCGTGA	ENSP00000516512.1:p.Lys50ThrfsTer?
ENST00000354171.13:c.532_533insCGCGTGA MANE Select	ENSP00000346103.7:p.Lys178ThrfsTer?
ENST00000589115.6:c.507_508insCGCGTGA	ENSP00000466872.3:p.Ser170ArgfsTer23
ENST00000354171.12:c.532_533insCGCGTGA	ENSP00000346103.7:p.Lys178ThrfsTer?
ENST00000585480.1:c.265_266insCGCGTGA	ENSP00000467900.1:p.Lys89ThrfsTer?
ENST00000587648.5:c.412_413insCGCGTGA	ENSP00000468349.1:p.Lys138ThrfsTer?
ENST00000588919.5:c.473_474insCGCGTGA	ENSP00000464989.3:p.Glu158AspfsTer3
ENST00000589115.5:c.507_508insCGCGTGA	ENSP00000466872.2:p.Ser170ArgfsTer23
ENST00000592940.2:n.903_904insCGCGTGA
ENST00000593032.5:c.512_513insCGCGTGA	ENSP00000465828.3:p.Glu171AspfsTer3
ENST00000611653.4:c.451_452insCGCGTGA	ENSP00000483655.1:p.Lys151ThrfsTer?
ENST00000616066.4:c.529_530insCGCGTGA	ENSP00000485000.1:p.Lys177ThrfsTer?
ENST00000622390.4:c.640_641insCGCGTGA	ENSP00000477503.1:p.Lys214ThrfsTer?
NM_001039847.2:c.554_555insCGCGTGA	NP_001034936.1:p.Glu185AspfsTer3
NM_001039848.2:c.643_644insCGCGTGA	NP_001034937.1:p.Lys215ThrfsTer?
NM_002085.4:c.532_533insCGCGTGA	NP_002076.2:p.Lys178ThrfsTer?
NM_001039848.3:c.643_644insCGCGTGA	NP_001034937.1:p.Lys215ThrfsTer?
NM_001039847.3:c.554_555insCGCGTGA	NP_001034936.1:p.Glu185AspfsTer3
NM_001039848.4:c.643_644insCGCGTGA	NP_001034937.1:p.Lys215ThrfsTer?
NM_001367832.1:c.451_452insCGCGTGA	NP_001354761.1:p.Lys151ThrfsTer?
NM_002085.5:c.532_533insCGCGTGA MANE Select	NP_002076.2:p.Lys178ThrfsTer?