Canonical Allele Identifier: CA2694424280

Gene: PSMD10

Linked Data

• gnomAD v4: X-108084936-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084936A>G , CM000685.2:g.108084936A>G	GRCh38
NC_000023.10:g.107328166A>G , CM000685.1:g.107328166A>G	GRCh37
NC_000023.9:g.107214822A>G	NCBI36
NG_012521.1:g.11683T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*38T>C MANE Select	ENSP00000217958.3:n.*38T>C
ENST00000217958.7:c.*38T>C	ENSP00000217958.3:n.*38T>C
ENST00000340200.5:c.620T>C	ENSP00000345963.5:n.620T>C
ENST00000361815.9:c.*184T>C	ENSP00000354906.5:n.*184T>C
ENST00000372295.5:c.*38T>C	ENSP00000361369.1:n.*38T>C
ENST00000372296.5:c.*184T>C	ENSP00000361370.1:n.*184T>C
NM_002814.3:c.*38T>C	NP_002805.1:n.*38T>C
NM_170750.2:c.*184T>C	NP_736606.1:n.*184T>C
NM_002814.4:c.*38T>C MANE Select	NP_002805.1:n.*38T>C
NM_170750.3:c.*184T>C	NP_736606.1:n.*184T>C