Canonical Allele Identifier: CA2694424179
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084742-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084742A>C , CM000685.2:g.108084742A>C GRCh38
NC_000023.10:g.107327972A>C , CM000685.1:g.107327972A>C GRCh37
NC_000023.9:g.107214628A>C NCBI36
NG_012521.1:g.11877T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*232T>G MANE Select ENSP00000217958.3:n.*232T>G
ENST00000217958.7:c.*232T>G ENSP00000217958.3:n.*232T>G
ENST00000372296.5:c.*378T>G ENSP00000361370.1:n.*378T>G
NM_002814.3:c.*232T>G NP_002805.1:n.*232T>G
NM_170750.2:c.*378T>G NP_736606.1:n.*378T>G
NM_002814.4:c.*232T>G MANE Select NP_002805.1:n.*232T>G
NM_170750.3:c.*378T>G NP_736606.1:n.*378T>G
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