Canonical Allele Identifier: CA2694424071
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084392-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084392T>G , CM000685.2:g.108084392T>G GRCh38
NC_000023.10:g.107327622T>G , CM000685.1:g.107327622T>G GRCh37
NC_000023.9:g.107214278T>G NCBI36
NG_012521.1:g.12227A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*582A>C MANE Select ENSP00000217958.3:n.*582A>C
ENST00000217958.7:c.*582A>C ENSP00000217958.3:n.*582A>C
NM_002814.3:c.*582A>C NP_002805.1:n.*582A>C
NM_170750.2:c.*728A>C NP_736606.1:n.*728A>C
NM_002814.4:c.*582A>C MANE Select NP_002805.1:n.*582A>C
NM_170750.3:c.*728A>C NP_736606.1:n.*728A>C
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