Canonical Allele Identifier: CA2694424096
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108084554-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084554A>T , CM000685.2:g.108084554A>T GRCh38
NC_000023.10:g.107327784A>T , CM000685.1:g.107327784A>T GRCh37
NC_000023.9:g.107214440A>T NCBI36
NG_012521.1:g.12065T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*420T>A MANE Select ENSP00000217958.3:n.*420T>A
ENST00000217958.7:c.*420T>A ENSP00000217958.3:n.*420T>A
NM_002814.3:c.*420T>A NP_002805.1:n.*420T>A
NM_170750.2:c.*566T>A NP_736606.1:n.*566T>A
NM_002814.4:c.*420T>A MANE Select NP_002805.1:n.*420T>A
NM_170750.3:c.*566T>A NP_736606.1:n.*566T>A
Search 100 bp 5'
Search 100 bp 3'