Canonical Allele Identifier: CA2572030798

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084965-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084965C>A , CM000685.2:g.108084965C>A	GRCh38
NC_000023.10:g.107328195C>A , CM000685.1:g.107328195C>A	GRCh37
NC_000023.9:g.107214851C>A	NCBI36
NG_012521.1:g.11654G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*9G>T MANE Select	ENSP00000217958.3:n.*9G>T
ENST00000217958.7:c.*9G>T	ENSP00000217958.3:n.*9G>T
ENST00000340200.5:c.591G>T	ENSP00000345963.5:n.591G>T
ENST00000361815.9:c.*155G>T	ENSP00000354906.5:n.*155G>T
ENST00000372295.5:c.*9G>T	ENSP00000361369.1:n.*9G>T
ENST00000372296.5:c.*155G>T	ENSP00000361370.1:n.*155G>T
NM_002814.3:c.*9G>T	NP_002805.1:n.*9G>T
NM_170750.2:c.*155G>T	NP_736606.1:n.*155G>T
NM_002814.4:c.*9G>T MANE Select	NP_002805.1:n.*9G>T
NM_170750.3:c.*155G>T	NP_736606.1:n.*155G>T