Canonical Allele Identifier: CA2450520321

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085012C= , CM000685.2:g.108085012C=	GRCh38
NC_000023.10:g.107328242C= , CM000685.1:g.107328242C=	GRCh37
NC_000023.9:g.107214898C=	NCBI36
NG_012521.1:g.11607G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.643G= MANE Select	ENSP00000217958.3:p.Gly215=
ENST00000217958.7:c.643G=	ENSP00000217958.3:p.Gly215=
ENST00000340200.5:c.544G=	ENSP00000345963.5:p.Gly182=
ENST00000361815.9:c.*108G=	ENSP00000354906.5:n.*108G=
ENST00000372295.5:c.520G=	ENSP00000361369.1:p.Gly174=
ENST00000372296.5:c.*108G=	ENSP00000361370.1:n.*108G=
NM_002814.3:c.643G=	NP_002805.1:p.Gly215=
NM_170750.2:c.*108G=	NP_736606.1:n.*108G=
NM_002814.4:c.643G= MANE Select	NP_002805.1:p.Gly215=
NM_170750.3:c.*108G=	NP_736606.1:n.*108G=