Canonical Allele Identifier: CA783225069

Gene: GPX4

Linked Data

• dbSNP Id: rs1184693350
• MyVariant Identifiers: chr19:g.1106241del (hg19) ; chr19:g.1106242del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106242del , CM000681.2:g.1106242del	GRCh38
NC_000019.9:g.1106241del , CM000681.1:g.1106241del	GRCh37
NC_000019.8:g.1057241del	NCBI36
NG_050621.1:g.7317del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.588del	ENSP00000473614.3:p.Asn196LysfsTer19
ENST00000593032.6:c.457del	ENSP00000465828.4:p.Cys153AlafsTer?
ENST00000706713.1:c.471del	ENSP00000516510.1:p.Asn157LysfsTer19
ENST00000706714.1:c.457del	ENSP00000516511.1:p.Cys153AlafsTer?
ENST00000706715.1:c.93del	ENSP00000516512.1:p.Asn31LysfsTer19
ENST00000354171.13:c.477del MANE Select	ENSP00000346103.7:p.Asn159LysfsTer19
ENST00000589115.6:c.477-158del	ENSP00000466872.3:n.477-158del
ENST00000354171.12:c.477del	ENSP00000346103.7:p.Asn159LysfsTer19
ENST00000585480.1:c.210del	ENSP00000467900.1:p.Asn70LysfsTer19
ENST00000587648.5:c.357del	ENSP00000468349.1:p.Asn119LysfsTer19
ENST00000588919.5:c.396del	ENSP00000464989.3:p.Asn132LysfsTer?
ENST00000589115.5:c.477-158del	ENSP00000466872.2:n.477-158del
ENST00000592940.2:n.848del
ENST00000593032.5:c.457del	ENSP00000465828.3:p.Cys153AlafsTer?
ENST00000611653.4:c.396del	ENSP00000483655.1:p.Asn132LysfsTer19
ENST00000616066.4:c.474del	ENSP00000485000.1:p.Asn158LysfsTer19
ENST00000622390.4:c.585del	ENSP00000477503.1:p.Asn195LysfsTer19
NM_001039847.2:c.477del	NP_001034936.1:p.Asn159LysfsTer?
NM_001039848.2:c.588del	NP_001034937.1:p.Asn196LysfsTer19
NM_002085.4:c.477del	NP_002076.2:p.Asn159LysfsTer19
NM_001039848.3:c.588del	NP_001034937.1:p.Asn196LysfsTer19
NM_001039847.3:c.477del	NP_001034936.1:p.Asn159LysfsTer?
NM_001039848.4:c.588del	NP_001034937.1:p.Asn196LysfsTer19
NM_001367832.1:c.396del	NP_001354761.1:p.Asn132LysfsTer19
NM_002085.5:c.477del MANE Select	NP_002076.2:p.Asn159LysfsTer19