Canonical Allele Identifier: CA2813238428

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105559_1105560insCCTGGGGGGGGGGGGGGGGGGGGG , CM000681.2:g.1105559_1105560insCCTGGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000019.9:g.1105558_1105559insCCTGGGGGGGGGGGGGGGGGGGGG , CM000681.1:g.1105558_1105559insCCTGGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000019.8:g.1056558_1056559insCCTGGGGGGGGGGGGGGGGGGGGG	NCBI36
NG_050621.1:g.6634_6635insCCTGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.435+49_435+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000473614.3:n.435+49_435+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000593032.6:c.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000465828.4:n.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000706713.1:c.318+49_318+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000516510.1:n.318+49_318+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000706714.1:c.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000516511.1:n.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000706715.1:c.-61+49_-61+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000516512.1:n.-61+49_-61+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000354171.13:c.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000346103.7:n.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000589115.6:c.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000466872.3:n.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000354171.12:c.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000346103.7:n.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000585362.6:c.435+49_435+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000473614.2:n.435+49_435+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000585480.1:c.57+49_57+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000467900.1:n.57+49_57+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000587648.5:c.204+49_204+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000468349.1:n.204+49_204+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000587932.2:n.258+49_258+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000588919.5:c.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000464989.3:n.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000589115.5:c.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000466872.2:n.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000592940.2:n.270+49_270+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000593032.5:c.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000465828.3:n.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000611653.4:c.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000483655.1:n.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000616066.4:c.321+49_321+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000485000.1:n.321+49_321+50insCCTGGGGGGGGGGGGGGGGGGGGG
ENST00000622390.4:c.432+49_432+50insCCTGGGGGGGGGGGGGGGGGGGGG	ENSP00000477503.1:n.432+49_432+50insCCTGGGGGGGGGGGGGGGGGGGGG
NM_001039847.2:c.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG	NP_001034936.1:n.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG
NM_001039848.2:c.435+49_435+50insCCTGGGGGGGGGGGGGGGGGGGGG	NP_001034937.1:n.435+49_435+50insCCTGGGGGGGGGGGGGGGGGGGGG
NM_002085.4:c.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG	NP_002076.2:n.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG
NM_001039848.3:c.435+49_435+50insCCTGGGGGGGGGGGGGGGGGGGGG	NP_001034937.1:n.435+49_435+50insCCTGGGGGGGGGGGGGGGGGGGGG
NM_001039847.3:c.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG	NP_001034936.1:n.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG
NM_001039848.4:c.435+49_435+50insCCTGGGGGGGGGGGGGGGGGGGGG	NP_001034937.1:n.435+49_435+50insCCTGGGGGGGGGGGGGGGGGGGGG
NM_001367832.1:c.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG	NP_001354761.1:n.243+49_243+50insCCTGGGGGGGGGGGGGGGGGGGGG
NM_002085.5:c.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG MANE Select	NP_002076.2:n.324+49_324+50insCCTGGGGGGGGGGGGGGGGGGGGG