Canonical Allele Identifier: CA9037469

Gene: GPX4

Linked Data

• dbSNP Id: rs765340250
• ExAC: 19:1106412 A / ATT
• gnomAD v2: 19-1106412-A-ATT
• gnomAD v4: 19-1106413-A-ATT
• MyVariant Identifiers: chr19:g.1106412_1106413insTT (hg19) ; chr19:g.1106413_1106414insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1106413_1106414insTT , CM000681.2:g.1106413_1106414insTT	GRCh38
NC_000019.9:g.1106412_1106413insTT , CM000681.1:g.1106412_1106413insTT	GRCh37
NC_000019.8:g.1057412_1057413insTT	NCBI36
NG_050621.1:g.7488_7489insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585362.7:c.626_627insTT	ENSP00000473614.3:p.Lys209AsnfsTer2
ENST00000593032.6:c.495_496insTT	ENSP00000465828.4:p.Glu166LeufsTer27
ENST00000706713.1:c.509_510insTT	ENSP00000516510.1:p.Lys170AsnfsTer2
ENST00000706714.1:c.495_496insTT	ENSP00000516511.1:p.Glu166LeufsTer27
ENST00000706715.1:c.131_132insTT	ENSP00000516512.1:p.Lys44AsnfsTer2
ENST00000354171.13:c.515_516insTT MANE Select	ENSP00000346103.7:p.Lys172AsnfsTer2
ENST00000589115.6:c.490_491insTT	ENSP00000466872.3:p.Arg164IlefsTer?
ENST00000354171.12:c.515_516insTT	ENSP00000346103.7:p.Lys172AsnfsTer2
ENST00000585480.1:c.248_249insTT	ENSP00000467900.1:p.Lys83AsnfsTer2
ENST00000587648.5:c.395_396insTT	ENSP00000468349.1:p.Lys132AsnfsTer2
ENST00000588919.5:c.456_457insTT	ENSP00000464989.3:p.Glu153LeufsTer27
ENST00000589115.5:c.490_491insTT	ENSP00000466872.2:p.Arg164IlefsTer?
ENST00000592940.2:n.886_887insTT
ENST00000593032.5:c.495_496insTT	ENSP00000465828.3:p.Glu166LeufsTer?
ENST00000611653.4:c.434_435insTT	ENSP00000483655.1:p.Lys145AsnfsTer2
ENST00000616066.4:c.512_513insTT	ENSP00000485000.1:p.Lys171AsnfsTer2
ENST00000622390.4:c.623_624insTT	ENSP00000477503.1:p.Lys208AsnfsTer2
NM_001039847.2:c.537_538insTT	NP_001034936.1:p.Glu180LeufsTer27
NM_001039848.2:c.626_627insTT	NP_001034937.1:p.Lys209AsnfsTer2
NM_002085.4:c.515_516insTT	NP_002076.2:p.Lys172AsnfsTer2
NM_001039848.3:c.626_627insTT	NP_001034937.1:p.Lys209AsnfsTer2
NM_001039847.3:c.537_538insTT	NP_001034936.1:p.Glu180LeufsTer27
NM_001039848.4:c.626_627insTT	NP_001034937.1:p.Lys209AsnfsTer2
NM_001367832.1:c.434_435insTT	NP_001354761.1:p.Lys145AsnfsTer2
NM_002085.5:c.515_516insTT MANE Select	NP_002076.2:p.Lys172AsnfsTer2