Canonical Allele Identifier: CA2588207611

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106058-G-GCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106058_1106059insCT , CM000681.2:g.1106058_1106059insCT	GRCh38
NC_000019.9:g.1106057_1106058insCT , CM000681.1:g.1106057_1106058insCT	GRCh37
NC_000019.8:g.1057057_1057058insCT	NCBI36
NG_050621.1:g.7133_7134insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588-184_588-183insCT	ENSP00000473614.3:n.588-184_588-183insCT
ENST00000593032.6:c.396-123_396-122insCT	ENSP00000465828.4:n.396-123_396-122insCT
ENST00000706713.1:c.471-184_471-183insCT	ENSP00000516510.1:n.471-184_471-183insCT
ENST00000706714.1:c.396-123_396-122insCT	ENSP00000516511.1:n.396-123_396-122insCT
ENST00000706715.1:c.93-184_93-183insCT	ENSP00000516512.1:n.93-184_93-183insCT
ENST00000354171.13:c.477-184_477-183insCT MANE Select	ENSP00000346103.7:n.477-184_477-183insCT
ENST00000589115.6:c.476+249_476+250insCT	ENSP00000466872.3:n.476+249_476+250insCT
ENST00000354171.12:c.477-184_477-183insCT	ENSP00000346103.7:n.477-184_477-183insCT
ENST00000585480.1:c.210-184_210-183insCT	ENSP00000467900.1:n.210-184_210-183insCT
ENST00000587648.5:c.357-184_357-183insCT	ENSP00000468349.1:n.357-184_357-183insCT
ENST00000588919.5:c.396-184_396-183insCT	ENSP00000464989.3:n.396-184_396-183insCT
ENST00000589115.5:c.476+249_476+250insCT	ENSP00000466872.2:n.476+249_476+250insCT
ENST00000592940.2:n.664_665insCT
ENST00000593032.5:c.396-123_396-122insCT	ENSP00000465828.3:n.396-123_396-122insCT
ENST00000611653.4:c.396-184_396-183insCT	ENSP00000483655.1:n.396-184_396-183insCT
ENST00000616066.4:c.474-184_474-183insCT	ENSP00000485000.1:n.474-184_474-183insCT
ENST00000622390.4:c.585-184_585-183insCT	ENSP00000477503.1:n.585-184_585-183insCT
NM_001039847.2:c.477-184_477-183insCT	NP_001034936.1:n.477-184_477-183insCT
NM_001039848.2:c.588-184_588-183insCT	NP_001034937.1:n.588-184_588-183insCT
NM_002085.4:c.477-184_477-183insCT	NP_002076.2:n.477-184_477-183insCT
NM_001039848.3:c.588-184_588-183insCT	NP_001034937.1:n.588-184_588-183insCT
NM_001039847.3:c.477-184_477-183insCT	NP_001034936.1:n.477-184_477-183insCT
NM_001039848.4:c.588-184_588-183insCT	NP_001034937.1:n.588-184_588-183insCT
NM_001367832.1:c.396-184_396-183insCT	NP_001354761.1:n.396-184_396-183insCT
NM_002085.5:c.477-184_477-183insCT MANE Select	NP_002076.2:n.477-184_477-183insCT