Canonical Allele Identifier: CA2813238558

Gene: GPX4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106462_1106541del , CM000681.2:g.1106462_1106541del	GRCh38
NC_000019.9:g.1106461_1106540del , CM000681.1:g.1106461_1106540del	GRCh37
NC_000019.8:g.1057461_1057540del	NCBI36
NG_050621.1:g.7537_7616del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.672+3_674del
ENST00000593032.6:c.541+3_543del
ENST00000706713.1:c.555+3_557del
ENST00000706714.1:c.541+3_543del
ENST00000706715.1:c.177+3_179del
ENST00000354171.13:c.561+3_563del
ENST00000589115.6:c.536+3_538del
ENST00000354171.12:c.561+3_563del
ENST00000585480.1:c.294+3_295-32del
ENST00000587648.5:c.441+3_443del
ENST00000588919.5:c.502+3_504del
ENST00000589115.5:c.536+3_538del
ENST00000592940.2:n.932+3_934del
ENST00000611653.4:c.480+3_482del
ENST00000616066.4:c.558+3_560del
ENST00000622390.4:c.669+3_671del
NM_001039847.2:c.583+3_585del
NM_001039848.2:c.672+3_674del
NM_002085.4:c.561+3_563del
NM_001039848.3:c.672+3_674del
NM_001039847.3:c.583+3_585del
NM_001039848.4:c.672+3_674del
NM_001367832.1:c.480+3_482del
NM_002085.5:c.561+3_563del