Canonical Allele Identifier: CA2450520307

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084964T= , CM000685.2:g.108084964T=	GRCh38
NC_000023.10:g.107328194T= , CM000685.1:g.107328194T=	GRCh37
NC_000023.9:g.107214850T=	NCBI36
NG_012521.1:g.11655A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*10A= MANE Select	ENSP00000217958.3:n.*10A=
ENST00000217958.7:c.*10A=	ENSP00000217958.3:n.*10A=
ENST00000340200.5:c.592A=	ENSP00000345963.5:n.592A=
ENST00000361815.9:c.*156A=	ENSP00000354906.5:n.*156A=
ENST00000372295.5:c.*10A=	ENSP00000361369.1:n.*10A=
ENST00000372296.5:c.*156A=	ENSP00000361370.1:n.*156A=
NM_002814.3:c.*10A=	NP_002805.1:n.*10A=
NM_170750.2:c.*156A=	NP_736606.1:n.*156A=
NM_002814.4:c.*10A= MANE Select	NP_002805.1:n.*10A=
NM_170750.3:c.*156A=	NP_736606.1:n.*156A=