Canonical Allele Identifier: CA2347156413
Gene: PRNP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4699379_4699427delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT , CM000682.2:g.4699379_4699427delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT GRCh38
NC_000020.10:g.4680025_4680073delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT , CM000682.1:g.4680025_4680073delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT GRCh37
NC_000020.9:g.4628025_4628073delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NCBI36
NG_009087.1:g.18229_18277delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000379440.9:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT MANE Select ENSP00000368752.4:p.Gly53=
ENST00000424424.2:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT ENSP00000411599.2:p.Gly53=
ENST00000457586.2:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT ENSP00000415284.2:p.Gly53=
ENST00000379440.8:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT ENSP00000368752.4:p.Gly53=
ENST00000424424.1:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT ENSP00000411599.1:p.Gly53=
ENST00000430350.2:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT ENSP00000399376.2:p.Gly53=
ENST00000457586.1:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT ENSP00000415284.1:p.Gly53=
NM_000311.3:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_000302.1:p.Gly53=
NM_001080121.1:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001073590.1:p.Gly53=
NM_001080122.1:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001073591.1:p.Gly53=
NM_001080123.1:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001073592.1:p.Gly53=
NM_001271561.1:c.70_118delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001258490.1:p.Arg24=
NM_183079.2:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_898902.1:p.Gly53=
NM_000311.4:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_000302.1:p.Gly53=
NM_001080121.2:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001073590.1:p.Gly53=
NM_001080122.2:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001073591.1:p.Gly53=
NM_001080123.2:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001073592.1:p.Gly53=
NM_001271561.2:c.70_118delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001258490.1:p.Arg24=
NM_183079.3:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_898902.1:p.Gly53=
NM_000311.5:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT MANE Select NP_000302.1:p.Gly53=
NM_001080121.3:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001073590.1:p.Gly53=
NM_001080122.3:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001073591.1:p.Gly53=
NM_001080123.3:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001073592.1:p.Gly53=
NM_001271561.3:c.70_118delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_001258490.1:p.Arg24=
NM_183079.4:c.159_207delinsCGGTGGTGGCTGGGGGCAGCCTCATGGTGGTGGCTGGGGGCAGCCTCAT NP_898902.1:p.Gly53=