Canonical Allele Identifier: CA333053252
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs202105475
gnomAD v3: X-108084678-G-C
gnomAD v4: X-108084678-G-C
MyVariant Identifiers: chrX:g.107327908G>C (hg19) chrX:g.108084678G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084678G>C , CM000685.2:g.108084678G>C GRCh38
NC_000023.10:g.107327908G>C , CM000685.1:g.107327908G>C GRCh37
NC_000023.9:g.107214564G>C NCBI36
NG_012521.1:g.11941C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*296C>G MANE Select ENSP00000217958.3:n.*296C>G
ENST00000217958.7:c.*296C>G ENSP00000217958.3:n.*296C>G
ENST00000372296.5:c.*442C>G ENSP00000361370.1:n.*442C>G
NM_002814.3:c.*296C>G NP_002805.1:n.*296C>G
NM_170750.2:c.*442C>G NP_736606.1:n.*442C>G
NM_002814.4:c.*296C>G MANE Select NP_002805.1:n.*296C>G
NM_170750.3:c.*442C>G NP_736606.1:n.*442C>G
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