Canonical Allele Identifier: CA2573157041
Gene: PRNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1562637
ClinVar RCV Id: RCV002204940

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4699604_4699605delinsTG , CM000682.2:g.4699604_4699605delinsTG GRCh38
NC_000020.10:g.4680250_4680251delinsTG , CM000682.1:g.4680250_4680251delinsTG GRCh37
NC_000020.9:g.4628250_4628251delinsTG NCBI36
NG_009087.1:g.18454_18455delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000379440.9:c.384_385delinsTG MANE Select ENSP00000368752.4:p.Met129Val
ENST00000424424.2:c.384_385delinsTG ENSP00000411599.2:p.Met129Val
ENST00000457586.2:c.384_385delinsTG ENSP00000415284.2:p.Met129Val
ENST00000379440.8:c.384_385delinsTG ENSP00000368752.4:p.Met129Val
ENST00000424424.1:c.384_385delinsTG ENSP00000411599.1:p.Met129Val
ENST00000430350.2:c.384_385delinsTG ENSP00000399376.2:p.Met129Val
ENST00000457586.1:c.384_385delinsTG ENSP00000415284.1:p.Met129Val
NM_000311.3:c.384_385delinsTG NP_000302.1:p.Met129Val
NM_001080121.1:c.384_385delinsTG NP_001073590.1:p.Met129Val
NM_001080122.1:c.384_385delinsTG NP_001073591.1:p.Met129Val
NM_001080123.1:c.384_385delinsTG NP_001073592.1:p.Met129Val
NM_001271561.1:c.*73_*74delinsTG NP_001258490.1:n.*73_*74delinsTG
NM_183079.2:c.384_385delinsTG NP_898902.1:p.Met129Val
NM_000311.4:c.384_385delinsTG NP_000302.1:p.Met129Val
NM_001080121.2:c.384_385delinsTG NP_001073590.1:p.Met129Val
NM_001080122.2:c.384_385delinsTG NP_001073591.1:p.Met129Val
NM_001080123.2:c.384_385delinsTG NP_001073592.1:p.Met129Val
NM_001271561.2:c.*73_*74delinsTG NP_001258490.1:n.*73_*74delinsTG
NM_183079.3:c.384_385delinsTG NP_898902.1:p.Met129Val
NM_000311.5:c.384_385delinsTG MANE Select NP_000302.1:p.Met129Val
NM_001080121.3:c.384_385delinsTG NP_001073590.1:p.Met129Val
NM_001080122.3:c.384_385delinsTG NP_001073591.1:p.Met129Val
NM_001080123.3:c.384_385delinsTG NP_001073592.1:p.Met129Val
NM_001271561.3:c.*73_*74delinsTG NP_001258490.1:n.*73_*74delinsTG
NM_183079.4:c.384_385delinsTG NP_898902.1:p.Met129Val