Canonical Allele Identifier: CA2588206319

Gene: GPX4

Linked Data

• gnomAD v4: 19-1104464-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104465del , CM000681.2:g.1104465del	GRCh38
NC_000019.9:g.1104464del , CM000681.1:g.1104464del	GRCh37
NC_000019.8:g.1055464del	NCBI36
NG_050621.1:g.5540del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593032.6:c.3+338del	ENSP00000465828.4:n.3+338del
ENST00000706713.1:c.84+338del	ENSP00000516510.1:n.84+338del
ENST00000706714.1:c.3+338del	ENSP00000516511.1:n.3+338del
ENST00000706715.1:c.-301+137del	ENSP00000516512.1:n.-301+137del
ENST00000354171.13:c.84+338del MANE Select	ENSP00000346103.7:n.84+338del
ENST00000589115.6:c.84+338del	ENSP00000466872.3:n.84+338del
ENST00000354171.12:c.84+338del	ENSP00000346103.7:n.84+338del
ENST00000585362.6:c.-270del	ENSP00000473614.2:n.-270del
ENST00000588919.5:c.3+338del	ENSP00000464989.3:n.3+338del
ENST00000589115.5:c.84+338del	ENSP00000466872.2:n.84+338del
ENST00000593032.5:c.3+338del	ENSP00000465828.3:n.3+338del
ENST00000611653.4:c.3+338del	ENSP00000483655.1:n.3+338del
ENST00000616066.4:c.84+338del	ENSP00000485000.1:n.84+338del
NM_001039847.2:c.84+338del	NP_001034936.1:n.84+338del
NM_002085.4:c.84+338del	NP_002076.2:n.84+338del
NM_001039847.3:c.84+338del	NP_001034936.1:n.84+338del
NM_001367832.1:c.3+338del	NP_001354761.1:n.3+338del
NM_002085.5:c.84+338del MANE Select	NP_002076.2:n.84+338del