Canonical Allele Identifier: CA2588207847

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106458-TGGTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106462_1106465del , CM000681.2:g.1106462_1106465del	GRCh38
NC_000019.9:g.1106461_1106464del , CM000681.1:g.1106461_1106464del	GRCh37
NC_000019.8:g.1057461_1057464del	NCBI36
NG_050621.1:g.7537_7540del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.672+3_672+6del
ENST00000593032.6:c.541+3_541+6del
ENST00000706713.1:c.555+3_555+6del
ENST00000706714.1:c.541+3_541+6del
ENST00000706715.1:c.177+3_177+6del
ENST00000354171.13:c.561+3_561+6del
ENST00000589115.6:c.536+3_536+6del
ENST00000354171.12:c.561+3_561+6del
ENST00000585480.1:c.294+3_294+6del
ENST00000587648.5:c.441+3_441+6del
ENST00000588919.5:c.502+3_502+6del
ENST00000589115.5:c.536+3_536+6del
ENST00000592940.2:n.932+3_932+6del
ENST00000611653.4:c.480+3_480+6del
ENST00000616066.4:c.558+3_558+6del
ENST00000622390.4:c.669+3_669+6del
NM_001039847.2:c.583+3_583+6del
NM_001039848.2:c.672+3_672+6del
NM_002085.4:c.561+3_561+6del
NM_001039848.3:c.672+3_672+6del
NM_001039847.3:c.583+3_583+6del
NM_001039848.4:c.672+3_672+6del
NM_001367832.1:c.480+3_480+6del
NM_002085.5:c.561+3_561+6del