Canonical Allele Identifier: CA2694424208
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084791-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084791T>C , CM000685.2:g.108084791T>C GRCh38
NC_000023.10:g.107328021T>C , CM000685.1:g.107328021T>C GRCh37
NC_000023.9:g.107214677T>C NCBI36
NG_012521.1:g.11828A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*183A>G MANE Select ENSP00000217958.3:n.*183A>G
ENST00000217958.7:c.*183A>G ENSP00000217958.3:n.*183A>G
ENST00000372295.5:c.*183A>G ENSP00000361369.1:n.*183A>G
ENST00000372296.5:c.*329A>G ENSP00000361370.1:n.*329A>G
NM_002814.3:c.*183A>G NP_002805.1:n.*183A>G
NM_170750.2:c.*329A>G NP_736606.1:n.*329A>G
NM_002814.4:c.*183A>G MANE Select NP_002805.1:n.*183A>G
NM_170750.3:c.*329A>G NP_736606.1:n.*329A>G
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