Canonical Allele Identifier: CA2450520328

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085033G= , CM000685.2:g.108085033G=	GRCh38
NC_000023.10:g.107328263G= , CM000685.1:g.107328263G=	GRCh37
NC_000023.9:g.107214919G=	NCBI36
NG_012521.1:g.11586C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.622C= MANE Select	ENSP00000217958.3:p.Pro208=
ENST00000217958.7:c.622C=	ENSP00000217958.3:p.Pro208=
ENST00000340200.5:c.523C=	ENSP00000345963.5:p.Pro175=
ENST00000361815.9:c.*87C=	ENSP00000354906.5:n.*87C=
ENST00000372295.5:c.499C=	ENSP00000361369.1:p.Pro167=
ENST00000372296.5:c.*87C=	ENSP00000361370.1:n.*87C=
NM_002814.3:c.622C=	NP_002805.1:p.Pro208=
NM_170750.2:c.*87C=	NP_736606.1:n.*87C=
NM_002814.4:c.622C= MANE Select	NP_002805.1:p.Pro208=
NM_170750.3:c.*87C=	NP_736606.1:n.*87C=