Canonical Allele Identifier: CA2694424100
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084568-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084568T>C , CM000685.2:g.108084568T>C GRCh38
NC_000023.10:g.107327798T>C , CM000685.1:g.107327798T>C GRCh37
NC_000023.9:g.107214454T>C NCBI36
NG_012521.1:g.12051A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*406A>G MANE Select ENSP00000217958.3:n.*406A>G
ENST00000217958.7:c.*406A>G ENSP00000217958.3:n.*406A>G
NM_002814.3:c.*406A>G NP_002805.1:n.*406A>G
NM_170750.2:c.*552A>G NP_736606.1:n.*552A>G
NM_002814.4:c.*406A>G MANE Select NP_002805.1:n.*406A>G
NM_170750.3:c.*552A>G NP_736606.1:n.*552A>G
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