Canonical Allele Identifier: CA2588207792

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106259-TCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106262_1106264del , CM000681.2:g.1106262_1106264del	GRCh38
NC_000019.9:g.1106261_1106263del , CM000681.1:g.1106261_1106263del	GRCh37
NC_000019.8:g.1057261_1057263del	NCBI36
NG_050621.1:g.7337_7339del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.608_610del	ENSP00000473614.3:p.Thr203del
ENST00000593032.6:c.477_479del	ENSP00000465828.4:p.His159del
ENST00000706713.1:c.491_493del	ENSP00000516510.1:p.Thr164del
ENST00000706714.1:c.477_479del	ENSP00000516511.1:p.His159del
ENST00000706715.1:c.113_115del	ENSP00000516512.1:p.Thr38del
ENST00000354171.13:c.497_499del MANE Select	ENSP00000346103.7:p.Thr166del
ENST00000589115.6:c.477-138_477-136del	ENSP00000466872.3:n.477-138_477-136del
ENST00000354171.12:c.497_499del	ENSP00000346103.7:p.Thr166del
ENST00000585480.1:c.230_232del	ENSP00000467900.1:p.Thr77del
ENST00000587648.5:c.377_379del	ENSP00000468349.1:p.Thr126del
ENST00000588919.5:c.416_418del	ENSP00000464989.3:p.Thr139del
ENST00000589115.5:c.477-138_477-136del	ENSP00000466872.2:n.477-138_477-136del
ENST00000592940.2:n.868_870del
ENST00000593032.5:c.477_479del	ENSP00000465828.3:p.His159del
ENST00000611653.4:c.416_418del	ENSP00000483655.1:p.Thr139del
ENST00000616066.4:c.494_496del	ENSP00000485000.1:p.Thr165del
ENST00000622390.4:c.605_607del	ENSP00000477503.1:p.Thr202del
NM_001039847.2:c.497_499del	NP_001034936.1:p.Thr166del
NM_001039848.2:c.608_610del	NP_001034937.1:p.Thr203del
NM_002085.4:c.497_499del	NP_002076.2:p.Thr166del
NM_001039848.3:c.608_610del	NP_001034937.1:p.Thr203del
NM_001039847.3:c.497_499del	NP_001034936.1:p.Thr166del
NM_001039848.4:c.608_610del	NP_001034937.1:p.Thr203del
NM_001367832.1:c.416_418del	NP_001354761.1:p.Thr139del
NM_002085.5:c.497_499del MANE Select	NP_002076.2:p.Thr166del