Canonical Allele Identifier: CA2531476264

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106193_1106300del , CM000681.2:g.1106193_1106300del	GRCh38
NC_000019.9:g.1106192_1106299del , CM000681.1:g.1106192_1106299del	GRCh37
NC_000019.8:g.1057192_1057299del	NCBI36
NG_050621.1:g.7268_7375del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-49_612+34del
ENST00000593032.6:c.408_481+34del
ENST00000706713.1:c.471-49_495+34del
ENST00000706714.1:c.408_481+34del
ENST00000706715.1:c.93-49_117+34del
ENST00000354171.13:c.477-49_501+34del
ENST00000589115.6:c.477-207_477-100del	ENSP00000466872.3:n.477-207_477-100del
ENST00000354171.12:c.477-49_501+34del
ENST00000585480.1:c.210-49_234+34del
ENST00000587648.5:c.357-49_381+34del
ENST00000588919.5:c.396-49_420+34del
ENST00000589115.5:c.477-207_477-100del	ENSP00000466872.2:n.477-207_477-100del
ENST00000592940.2:n.799_872+34del
ENST00000593032.5:c.408_481+34del
ENST00000611653.4:c.396-49_420+34del
ENST00000616066.4:c.474-49_498+34del
ENST00000622390.4:c.585-49_609+34del
NM_001039847.2:c.477-49_501+34del
NM_001039848.2:c.588-49_612+34del
NM_002085.4:c.477-49_501+34del
NM_001039848.3:c.588-49_612+34del
NM_001039847.3:c.477-49_501+34del
NM_001039848.4:c.588-49_612+34del
NM_001367832.1:c.396-49_420+34del
NM_002085.5:c.477-49_501+34del