Canonical Allele Identifier: CA2694424267

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084912-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084912T>C , CM000685.2:g.108084912T>C	GRCh38
NC_000023.10:g.107328142T>C , CM000685.1:g.107328142T>C	GRCh37
NC_000023.9:g.107214798T>C	NCBI36
NG_012521.1:g.11707A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*62A>G MANE Select	ENSP00000217958.3:n.*62A>G
ENST00000217958.7:c.*62A>G	ENSP00000217958.3:n.*62A>G
ENST00000340200.5:c.644A>G	ENSP00000345963.5:n.644A>G
ENST00000361815.9:c.*208A>G	ENSP00000354906.5:n.*208A>G
ENST00000372295.5:c.*62A>G	ENSP00000361369.1:n.*62A>G
ENST00000372296.5:c.*208A>G	ENSP00000361370.1:n.*208A>G
NM_002814.3:c.*62A>G	NP_002805.1:n.*62A>G
NM_170750.2:c.*208A>G	NP_736606.1:n.*208A>G
NM_002814.4:c.*62A>G MANE Select	NP_002805.1:n.*62A>G
NM_170750.3:c.*208A>G	NP_736606.1:n.*208A>G