Canonical Allele Identifier: CA2838511061

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106649dup , CM000681.2:g.1106649dup	GRCh38
NC_000019.9:g.1106648dup , CM000681.1:g.1106648dup	GRCh37
NC_000019.8:g.1057648dup	NCBI36
NG_050621.1:g.7724dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.*77dup	ENSP00000473614.3:n.*77dup
ENST00000593032.6:c.651dup	ENSP00000465828.4:p.Cys218LeufsTer?
ENST00000706713.1:c.*77dup	ENSP00000516510.1:n.*77dup
ENST00000706714.1:c.651dup	ENSP00000516511.1:p.Cys218LeufsTer?
ENST00000706715.1:c.*77dup	ENSP00000516512.1:n.*77dup
ENST00000354171.13:c.*77dup MANE Select	ENSP00000346103.7:n.*77dup
ENST00000589115.6:c.*103dup	ENSP00000466872.3:n.*103dup
ENST00000354171.12:c.*77dup	ENSP00000346103.7:n.*77dup
ENST00000585480.1:c.371dup	ENSP00000467900.1:p.Ala125CysfsTer?
ENST00000588919.5:c.612dup	ENSP00000464989.3:p.Cys205LeufsTer?
ENST00000589115.5:c.*103dup	ENSP00000466872.2:n.*103dup
ENST00000592940.2:n.1042dup
ENST00000611653.4:c.*77dup	ENSP00000483655.1:n.*77dup
ENST00000616066.4:c.*77dup	ENSP00000485000.1:n.*77dup
ENST00000622390.4:c.*77dup	ENSP00000477503.1:n.*77dup
NM_001039847.2:c.*9dup	NP_001034936.1:n.*9dup
NM_001039848.2:c.*77dup	NP_001034937.1:n.*77dup
NM_002085.4:c.*77dup	NP_002076.2:n.*77dup
NM_001039848.3:c.*77dup	NP_001034937.1:n.*77dup
NM_001039847.3:c.*9dup	NP_001034936.1:n.*9dup
NM_001039848.4:c.*77dup	NP_001034937.1:n.*77dup
NM_001367832.1:c.*77dup	NP_001354761.1:n.*77dup
NM_002085.5:c.*77dup MANE Select	NP_002076.2:n.*77dup