Canonical Allele Identifier: CA2813238386

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105550_1105551insGGGGGGTGGG , CM000681.2:g.1105550_1105551insGGGGGGTGGG	GRCh38
NC_000019.9:g.1105549_1105550insGGGGGGTGGG , CM000681.1:g.1105549_1105550insGGGGGGTGGG	GRCh37
NC_000019.8:g.1056549_1056550insGGGGGGTGGG	NCBI36
NG_050621.1:g.6625_6626insGGGGGGTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.435+40_435+41insGGGGGGTGGG	ENSP00000473614.3:n.435+40_435+41insGGGGGGTGGG
ENST00000593032.6:c.243+40_243+41insGGGGGGTGGG	ENSP00000465828.4:n.243+40_243+41insGGGGGGTGGG
ENST00000706713.1:c.318+40_318+41insGGGGGGTGGG	ENSP00000516510.1:n.318+40_318+41insGGGGGGTGGG
ENST00000706714.1:c.243+40_243+41insGGGGGGTGGG	ENSP00000516511.1:n.243+40_243+41insGGGGGGTGGG
ENST00000706715.1:c.-61+40_-61+41insGGGGGGTGGG	ENSP00000516512.1:n.-61+40_-61+41insGGGGGGTGGG
ENST00000354171.13:c.324+40_324+41insGGGGGGTGGG MANE Select	ENSP00000346103.7:n.324+40_324+41insGGGGGGTGGG
ENST00000589115.6:c.324+40_324+41insGGGGGGTGGG	ENSP00000466872.3:n.324+40_324+41insGGGGGGTGGG
ENST00000354171.12:c.324+40_324+41insGGGGGGTGGG	ENSP00000346103.7:n.324+40_324+41insGGGGGGTGGG
ENST00000585362.6:c.435+40_435+41insGGGGGGTGGG	ENSP00000473614.2:n.435+40_435+41insGGGGGGTGGG
ENST00000585480.1:c.57+40_57+41insGGGGGGTGGG	ENSP00000467900.1:n.57+40_57+41insGGGGGGTGGG
ENST00000587648.5:c.204+40_204+41insGGGGGGTGGG	ENSP00000468349.1:n.204+40_204+41insGGGGGGTGGG
ENST00000587932.2:n.258+40_258+41insGGGGGGTGGG
ENST00000588919.5:c.243+40_243+41insGGGGGGTGGG	ENSP00000464989.3:n.243+40_243+41insGGGGGGTGGG
ENST00000589115.5:c.324+40_324+41insGGGGGGTGGG	ENSP00000466872.2:n.324+40_324+41insGGGGGGTGGG
ENST00000592940.2:n.270+40_270+41insGGGGGGTGGG
ENST00000593032.5:c.243+40_243+41insGGGGGGTGGG	ENSP00000465828.3:n.243+40_243+41insGGGGGGTGGG
ENST00000611653.4:c.243+40_243+41insGGGGGGTGGG	ENSP00000483655.1:n.243+40_243+41insGGGGGGTGGG
ENST00000616066.4:c.321+40_321+41insGGGGGGTGGG	ENSP00000485000.1:n.321+40_321+41insGGGGGGTGGG
ENST00000622390.4:c.432+40_432+41insGGGGGGTGGG	ENSP00000477503.1:n.432+40_432+41insGGGGGGTGGG
NM_001039847.2:c.324+40_324+41insGGGGGGTGGG	NP_001034936.1:n.324+40_324+41insGGGGGGTGGG
NM_001039848.2:c.435+40_435+41insGGGGGGTGGG	NP_001034937.1:n.435+40_435+41insGGGGGGTGGG
NM_002085.4:c.324+40_324+41insGGGGGGTGGG	NP_002076.2:n.324+40_324+41insGGGGGGTGGG
NM_001039848.3:c.435+40_435+41insGGGGGGTGGG	NP_001034937.1:n.435+40_435+41insGGGGGGTGGG
NM_001039847.3:c.324+40_324+41insGGGGGGTGGG	NP_001034936.1:n.324+40_324+41insGGGGGGTGGG
NM_001039848.4:c.435+40_435+41insGGGGGGTGGG	NP_001034937.1:n.435+40_435+41insGGGGGGTGGG
NM_001367832.1:c.243+40_243+41insGGGGGGTGGG	NP_001354761.1:n.243+40_243+41insGGGGGGTGGG
NM_002085.5:c.324+40_324+41insGGGGGGTGGG MANE Select	NP_002076.2:n.324+40_324+41insGGGGGGTGGG