Canonical Allele Identifier: CA2694424197
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084774-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084774A>G , CM000685.2:g.108084774A>G GRCh38
NC_000023.10:g.107328004A>G , CM000685.1:g.107328004A>G GRCh37
NC_000023.9:g.107214660A>G NCBI36
NG_012521.1:g.11845T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*200T>C MANE Select ENSP00000217958.3:n.*200T>C
ENST00000217958.7:c.*200T>C ENSP00000217958.3:n.*200T>C
ENST00000372296.5:c.*346T>C ENSP00000361370.1:n.*346T>C
NM_002814.3:c.*200T>C NP_002805.1:n.*200T>C
NM_170750.2:c.*346T>C NP_736606.1:n.*346T>C
NM_002814.4:c.*200T>C MANE Select NP_002805.1:n.*200T>C
NM_170750.3:c.*346T>C NP_736606.1:n.*346T>C
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