Canonical Allele Identifier: CA2579673973

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084953-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084954dup , CM000685.2:g.108084954dup	GRCh38
NC_000023.10:g.107328184dup , CM000685.1:g.107328184dup	GRCh37
NC_000023.9:g.107214840dup	NCBI36
NG_012521.1:g.11665dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*20dup MANE Select	ENSP00000217958.3:n.*20dup
ENST00000217958.7:c.*20dup	ENSP00000217958.3:n.*20dup
ENST00000340200.5:c.602dup	ENSP00000345963.5:n.602dup
ENST00000361815.9:c.*166dup	ENSP00000354906.5:n.*166dup
ENST00000372295.5:c.*20dup	ENSP00000361369.1:n.*20dup
ENST00000372296.5:c.*166dup	ENSP00000361370.1:n.*166dup
NM_002814.3:c.*20dup	NP_002805.1:n.*20dup
NM_170750.2:c.*166dup	NP_736606.1:n.*166dup
NM_002814.4:c.*20dup MANE Select	NP_002805.1:n.*20dup
NM_170750.3:c.*166dup	NP_736606.1:n.*166dup