Canonical Allele Identifier: CA509567675
Gene: PRNP HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.4680043G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4699397G>A , CM000682.2:g.4699397G>A GRCh38
NC_000020.10:g.4680043G>A , CM000682.1:g.4680043G>A GRCh37
NC_000020.9:g.4628043G>A NCBI36
NG_009087.1:g.18247G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379440.9:c.177G>A MANE Select ENSP00000368752.4:p.Gln59=
ENST00000424424.2:c.177G>A ENSP00000411599.2:p.Gln59=
ENST00000457586.2:c.177G>A ENSP00000415284.2:p.Gln59=
ENST00000379440.8:c.177G>A ENSP00000368752.4:p.Gln59=
ENST00000424424.1:c.177G>A ENSP00000411599.1:p.Gln59=
ENST00000430350.2:c.177G>A ENSP00000399376.2:p.Gln59=
ENST00000457586.1:c.177G>A ENSP00000415284.1:p.Gln59=
NM_000311.3:c.177G>A NP_000302.1:p.Gln59=
NM_001080121.1:c.177G>A NP_001073590.1:p.Gln59=
NM_001080122.1:c.177G>A NP_001073591.1:p.Gln59=
NM_001080123.1:c.177G>A NP_001073592.1:p.Gln59=
NM_001271561.1:c.88G>A NP_001258490.1:p.Ala30Thr
NM_183079.2:c.177G>A NP_898902.1:p.Gln59=
NM_000311.4:c.177G>A NP_000302.1:p.Gln59=
NM_001080121.2:c.177G>A NP_001073590.1:p.Gln59=
NM_001080122.2:c.177G>A NP_001073591.1:p.Gln59=
NM_001080123.2:c.177G>A NP_001073592.1:p.Gln59=
NM_001271561.2:c.88G>A NP_001258490.1:p.Ala30Thr
NM_183079.3:c.177G>A NP_898902.1:p.Gln59=
NM_000311.5:c.177G>A MANE Select NP_000302.1:p.Gln59=
NM_001080121.3:c.177G>A NP_001073590.1:p.Gln59=
NM_001080122.3:c.177G>A NP_001073591.1:p.Gln59=
NM_001080123.3:c.177G>A NP_001073592.1:p.Gln59=
NM_001271561.3:c.88G>A NP_001258490.1:p.Ala30Thr
NM_183079.4:c.177G>A NP_898902.1:p.Gln59=