Canonical Allele Identifier: CA2576545153

Gene: GPX4

Linked Data

• gnomAD v4: 19-1106250-AGTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106252_1106254del , CM000681.2:g.1106252_1106254del	GRCh38
NC_000019.9:g.1106251_1106253del , CM000681.1:g.1106251_1106253del	GRCh37
NC_000019.8:g.1057251_1057253del	NCBI36
NG_050621.1:g.7327_7329del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.598_600del	ENSP00000473614.3:p.Trp200del
ENST00000593032.6:c.467_469del	ENSP00000465828.4:p.Val156del
ENST00000706713.1:c.481_483del	ENSP00000516510.1:p.Trp161del
ENST00000706714.1:c.467_469del	ENSP00000516511.1:p.Val156del
ENST00000706715.1:c.103_105del	ENSP00000516512.1:p.Trp35del
ENST00000354171.13:c.487_489del MANE Select	ENSP00000346103.7:p.Trp163del
ENST00000589115.6:c.477-148_477-146del	ENSP00000466872.3:n.477-148_477-146del
ENST00000354171.12:c.487_489del	ENSP00000346103.7:p.Trp163del
ENST00000585480.1:c.220_222del	ENSP00000467900.1:p.Trp74del
ENST00000587648.5:c.367_369del	ENSP00000468349.1:p.Trp123del
ENST00000588919.5:c.406_408del	ENSP00000464989.3:p.Trp136del
ENST00000589115.5:c.477-148_477-146del	ENSP00000466872.2:n.477-148_477-146del
ENST00000592940.2:n.858_860del
ENST00000593032.5:c.467_469del	ENSP00000465828.3:p.Val156del
ENST00000611653.4:c.406_408del	ENSP00000483655.1:p.Trp136del
ENST00000616066.4:c.484_486del	ENSP00000485000.1:p.Trp162del
ENST00000622390.4:c.595_597del	ENSP00000477503.1:p.Trp199del
NM_001039847.2:c.487_489del	NP_001034936.1:p.Trp163del
NM_001039848.2:c.598_600del	NP_001034937.1:p.Trp200del
NM_002085.4:c.487_489del	NP_002076.2:p.Trp163del
NM_001039848.3:c.598_600del	NP_001034937.1:p.Trp200del
NM_001039847.3:c.487_489del	NP_001034936.1:p.Trp163del
NM_001039848.4:c.598_600del	NP_001034937.1:p.Trp200del
NM_001367832.1:c.406_408del	NP_001354761.1:p.Trp136del
NM_002085.5:c.487_489del MANE Select	NP_002076.2:p.Trp163del