Canonical Allele Identifier: CA2450520293

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084896C= , CM000685.2:g.108084896C=	GRCh38
NC_000023.10:g.107328126C= , CM000685.1:g.107328126C=	GRCh37
NC_000023.9:g.107214782C=	NCBI36
NG_012521.1:g.11723G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217958.8:c.*78G= MANE Select	ENSP00000217958.3:n.*78G=
ENST00000217958.7:c.*78G=	ENSP00000217958.3:n.*78G=
ENST00000340200.5:c.660G=	ENSP00000345963.5:n.660G=
ENST00000361815.9:c.*224G=	ENSP00000354906.5:n.*224G=
ENST00000372295.5:c.*78G=	ENSP00000361369.1:n.*78G=
ENST00000372296.5:c.*224G=	ENSP00000361370.1:n.*224G=
NM_002814.3:c.*78G=	NP_002805.1:n.*78G=
NM_170750.2:c.*224G=	NP_736606.1:n.*224G=
NM_002814.4:c.*78G= MANE Select	NP_002805.1:n.*78G=
NM_170750.3:c.*224G=	NP_736606.1:n.*224G=