Canonical Allele Identifier: CA2694424095
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084548-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084548T>C , CM000685.2:g.108084548T>C GRCh38
NC_000023.10:g.107327778T>C , CM000685.1:g.107327778T>C GRCh37
NC_000023.9:g.107214434T>C NCBI36
NG_012521.1:g.12071A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*426A>G MANE Select ENSP00000217958.3:n.*426A>G
ENST00000217958.7:c.*426A>G ENSP00000217958.3:n.*426A>G
NM_002814.3:c.*426A>G NP_002805.1:n.*426A>G
NM_170750.2:c.*572A>G NP_736606.1:n.*572A>G
NM_002814.4:c.*426A>G MANE Select NP_002805.1:n.*426A>G
NM_170750.3:c.*572A>G NP_736606.1:n.*572A>G
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