Canonical Allele Identifier: CA2588205833

Gene: GPX4

Linked Data

• gnomAD v4: 19-1104060-TTTGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1104061_1104064del , CM000681.2:g.1104061_1104064del	GRCh38
NC_000019.9:g.1104060_1104063del , CM000681.1:g.1104060_1104063del	GRCh37
NC_000019.8:g.1055060_1055063del	NCBI36
NG_050621.1:g.5136_5139del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706713.1:c.18_21del	ENSP00000516510.1:p.Cys7AlafsTer3
ENST00000354171.13:c.18_21del MANE Select	ENSP00000346103.7:p.Cys7AlafsTer3
ENST00000589115.6:c.18_21del	ENSP00000466872.3:p.Cys7AlafsTer3
ENST00000354171.12:c.18_21del	ENSP00000346103.7:p.Cys7AlafsTer3
ENST00000589115.5:c.18_21del	ENSP00000466872.2:p.Cys7AlafsTer3
ENST00000611653.4:c.-64_-61del	ENSP00000483655.1:n.-64_-61del
ENST00000616066.4:c.18_21del	ENSP00000485000.1:p.Cys7AlafsTer3
NM_001039847.2:c.18_21del	NP_001034936.1:p.Cys7AlafsTer3
NM_002085.4:c.18_21del	NP_002076.2:p.Cys7AlafsTer3
NM_001039847.3:c.18_21del	NP_001034936.1:p.Cys7AlafsTer3
NM_001367832.1:c.-64_-61del	NP_001354761.1:n.-64_-61del
NM_002085.5:c.18_21del MANE Select	NP_002076.2:p.Cys7AlafsTer3