Canonical Allele Identifier: CA2694424258
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084880-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084880C>G , CM000685.2:g.108084880C>G GRCh38
NC_000023.10:g.107328110C>G , CM000685.1:g.107328110C>G GRCh37
NC_000023.9:g.107214766C>G NCBI36
NG_012521.1:g.11739G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*94G>C MANE Select ENSP00000217958.3:n.*94G>C
ENST00000217958.7:c.*94G>C ENSP00000217958.3:n.*94G>C
ENST00000340200.5:c.676G>C ENSP00000345963.5:n.676G>C
ENST00000361815.9:c.*240G>C ENSP00000354906.5:n.*240G>C
ENST00000372295.5:c.*94G>C ENSP00000361369.1:n.*94G>C
ENST00000372296.5:c.*240G>C ENSP00000361370.1:n.*240G>C
NM_002814.3:c.*94G>C NP_002805.1:n.*94G>C
NM_170750.2:c.*240G>C NP_736606.1:n.*240G>C
NM_002814.4:c.*94G>C MANE Select NP_002805.1:n.*94G>C
NM_170750.3:c.*240G>C NP_736606.1:n.*240G>C
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