Canonical Allele Identifier: CA2347156477

Gene: PRNP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4699483G= , CM000682.2:g.4699483G=	GRCh38
NC_000020.10:g.4680129G= , CM000682.1:g.4680129G=	GRCh37
NC_000020.9:g.4628129G=	NCBI36
NG_009087.1:g.18333G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379440.9:c.263G= MANE Select	ENSP00000368752.4:p.Gly88=
ENST00000424424.2:c.263G=	ENSP00000411599.2:p.Gly88=
ENST00000457586.2:c.263G=	ENSP00000415284.2:p.Gly88=
ENST00000379440.8:c.263G=	ENSP00000368752.4:p.Gly88=
ENST00000424424.1:c.263G=	ENSP00000411599.1:p.Gly88=
ENST00000430350.2:c.263G=	ENSP00000399376.2:p.Gly88=
ENST00000457586.1:c.263G=	ENSP00000415284.1:p.Gly88=
NM_000311.3:c.263G=	NP_000302.1:p.Gly88=
NM_001080121.1:c.263G=	NP_001073590.1:p.Gly88=
NM_001080122.1:c.263G=	NP_001073591.1:p.Gly88=
NM_001080123.1:c.263G=	NP_001073592.1:p.Gly88=
NM_001271561.1:c.174G=	NP_001258490.1:p.Trp58=
NM_183079.2:c.263G=	NP_898902.1:p.Gly88=
NM_000311.4:c.263G=	NP_000302.1:p.Gly88=
NM_001080121.2:c.263G=	NP_001073590.1:p.Gly88=
NM_001080122.2:c.263G=	NP_001073591.1:p.Gly88=
NM_001080123.2:c.263G=	NP_001073592.1:p.Gly88=
NM_001271561.2:c.174G=	NP_001258490.1:p.Trp58=
NM_183079.3:c.263G=	NP_898902.1:p.Gly88=
NM_000311.5:c.263G= MANE Select	NP_000302.1:p.Gly88=
NM_001080121.3:c.263G=	NP_001073590.1:p.Gly88=
NM_001080122.3:c.263G=	NP_001073591.1:p.Gly88=
NM_001080123.3:c.263G=	NP_001073592.1:p.Gly88=
NM_001271561.3:c.174G=	NP_001258490.1:p.Trp58=
NM_183079.4:c.263G=	NP_898902.1:p.Gly88=