Canonical Allele Identifier: CA2347156587

Gene: PRNP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.4699733C= , CM000682.2:g.4699733C=	GRCh38
NC_000020.10:g.4680379C= , CM000682.1:g.4680379C=	GRCh37
NC_000020.9:g.4628379C=	NCBI36
NG_009087.1:g.18583C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379440.9:c.513C= MANE Select	ENSP00000368752.4:p.Asn171=
ENST00000424424.2:c.513C=	ENSP00000411599.2:p.Asn171=
ENST00000457586.2:c.513C=	ENSP00000415284.2:p.Asn171=
ENST00000379440.8:c.513C=	ENSP00000368752.4:p.Asn171=
ENST00000424424.1:c.513C=	ENSP00000411599.1:p.Asn171=
ENST00000430350.2:c.513C=	ENSP00000399376.2:p.Asn171=
ENST00000457586.1:c.513C=	ENSP00000415284.1:p.Asn171=
NM_000311.3:c.513C=	NP_000302.1:p.Asn171=
NM_001080121.1:c.513C=	NP_001073590.1:p.Asn171=
NM_001080122.1:c.513C=	NP_001073591.1:p.Asn171=
NM_001080123.1:c.513C=	NP_001073592.1:p.Asn171=
NM_001271561.1:c.*202C=	NP_001258490.1:n.*202C=
NM_183079.2:c.513C=	NP_898902.1:p.Asn171=
NM_000311.4:c.513C=	NP_000302.1:p.Asn171=
NM_001080121.2:c.513C=	NP_001073590.1:p.Asn171=
NM_001080122.2:c.513C=	NP_001073591.1:p.Asn171=
NM_001080123.2:c.513C=	NP_001073592.1:p.Asn171=
NM_001271561.2:c.*202C=	NP_001258490.1:n.*202C=
NM_183079.3:c.513C=	NP_898902.1:p.Asn171=
NM_000311.5:c.513C= MANE Select	NP_000302.1:p.Asn171=
NM_001080121.3:c.513C=	NP_001073590.1:p.Asn171=
NM_001080122.3:c.513C=	NP_001073591.1:p.Asn171=
NM_001080123.3:c.513C=	NP_001073592.1:p.Asn171=
NM_001271561.3:c.*202C=	NP_001258490.1:n.*202C=
NM_183079.4:c.513C=	NP_898902.1:p.Asn171=