Canonical Allele Identifier: CA333053298

Gene: PSMD10

Linked Data

• dbSNP Id: rs939787387
• gnomAD v3: X-108084922-G-C
• gnomAD v4: X-108084922-G-C
• MyVariant Identifiers: chrX:g.107328152G>C (hg19) ; chrX:g.108084922G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084922G>C , CM000685.2:g.108084922G>C	GRCh38
NC_000023.10:g.107328152G>C , CM000685.1:g.107328152G>C	GRCh37
NC_000023.9:g.107214808G>C	NCBI36
NG_012521.1:g.11697C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*52C>G MANE Select	ENSP00000217958.3:n.*52C>G
ENST00000217958.7:c.*52C>G	ENSP00000217958.3:n.*52C>G
ENST00000340200.5:c.634C>G	ENSP00000345963.5:n.634C>G
ENST00000361815.9:c.*198C>G	ENSP00000354906.5:n.*198C>G
ENST00000372295.5:c.*52C>G	ENSP00000361369.1:n.*52C>G
ENST00000372296.5:c.*198C>G	ENSP00000361370.1:n.*198C>G
NM_002814.3:c.*52C>G	NP_002805.1:n.*52C>G
NM_170750.2:c.*198C>G	NP_736606.1:n.*198C>G
NM_002814.4:c.*52C>G MANE Select	NP_002805.1:n.*52C>G
NM_170750.3:c.*198C>G	NP_736606.1:n.*198C>G