Canonical Allele Identifier: CA631018784

Gene: GPX4

Linked Data

• dbSNP Id: rs1486586840
• gnomAD v2: 19-1105733-GCGTGAA-G
• gnomAD v4: 19-1105734-GCGTGAA-G
• MyVariant Identifiers: chr19:g.1105734_1105739del (hg19) ; chr19:g.1105735_1105740del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1105737_1105742del , CM000681.2:g.1105737_1105742del	GRCh38
NC_000019.9:g.1105736_1105741del , CM000681.1:g.1105736_1105741del	GRCh37
NC_000019.8:g.1056736_1056741del	NCBI36
NG_050621.1:g.6812_6817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.515_520del	ENSP00000473614.3:p.Val172_Asn173del
ENST00000593032.6:c.323_328del	ENSP00000465828.4:p.Val108_Asn109del
ENST00000706713.1:c.398_403del	ENSP00000516510.1:p.Val133_Asn134del
ENST00000706714.1:c.323_328del	ENSP00000516511.1:p.Val108_Asn109del
ENST00000706715.1:c.20_25del	ENSP00000516512.1:p.Val7_Asn8del
ENST00000354171.13:c.404_409del MANE Select	ENSP00000346103.7:p.Val135_Asn136del
ENST00000589115.6:c.404_409del	ENSP00000466872.3:p.Val135_Asn136del
ENST00000354171.12:c.404_409del	ENSP00000346103.7:p.Val135_Asn136del
ENST00000585362.6:c.515_520del	ENSP00000473614.2:p.Val172_Asn173del
ENST00000585480.1:c.137_142del	ENSP00000467900.1:p.Val46_Asn47del
ENST00000587648.5:c.284_289del	ENSP00000468349.1:p.Val95_Asn96del
ENST00000588919.5:c.323_328del	ENSP00000464989.3:p.Val108_Asn109del
ENST00000589115.5:c.404_409del	ENSP00000466872.2:p.Val135_Asn136del
ENST00000592940.2:n.343_348del
ENST00000593032.5:c.323_328del	ENSP00000465828.3:p.Val108_Asn109del
ENST00000611653.4:c.323_328del	ENSP00000483655.1:p.Val108_Asn109del
ENST00000616066.4:c.401_406del	ENSP00000485000.1:p.Val134_Asn135del
ENST00000622390.4:c.512_517del	ENSP00000477503.1:p.Val171_Asn172del
NM_001039847.2:c.404_409del	NP_001034936.1:p.Val135_Asn136del
NM_001039848.2:c.515_520del	NP_001034937.1:p.Val172_Asn173del
NM_002085.4:c.404_409del	NP_002076.2:p.Val135_Asn136del
NM_001039848.3:c.515_520del	NP_001034937.1:p.Val172_Asn173del
NM_001039847.3:c.404_409del	NP_001034936.1:p.Val135_Asn136del
NM_001039848.4:c.515_520del	NP_001034937.1:p.Val172_Asn173del
NM_001367832.1:c.323_328del	NP_001354761.1:p.Val108_Asn109del
NM_002085.5:c.404_409del MANE Select	NP_002076.2:p.Val135_Asn136del