Canonical Allele Identifier: CA2450520299

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084922G= , CM000685.2:g.108084922G=	GRCh38
NC_000023.10:g.107328152G= , CM000685.1:g.107328152G=	GRCh37
NC_000023.9:g.107214808G=	NCBI36
NG_012521.1:g.11697C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*52C= MANE Select	ENSP00000217958.3:n.*52C=
ENST00000217958.7:c.*52C=	ENSP00000217958.3:n.*52C=
ENST00000340200.5:c.634C=	ENSP00000345963.5:n.634C=
ENST00000361815.9:c.*198C=	ENSP00000354906.5:n.*198C=
ENST00000372295.5:c.*52C=	ENSP00000361369.1:n.*52C=
ENST00000372296.5:c.*198C=	ENSP00000361370.1:n.*198C=
NM_002814.3:c.*52C=	NP_002805.1:n.*52C=
NM_170750.2:c.*198C=	NP_736606.1:n.*198C=
NM_002814.4:c.*52C= MANE Select	NP_002805.1:n.*52C=
NM_170750.3:c.*198C=	NP_736606.1:n.*198C=