Canonical Allele Identifier: CA2450520209
Gene: PSMD10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084627C= , CM000685.2:g.108084627C= GRCh38
NC_000023.10:g.107327857C= , CM000685.1:g.107327857C= GRCh37
NC_000023.9:g.107214513C= NCBI36
NG_012521.1:g.11992G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*347G= MANE Select ENSP00000217958.3:n.*347G=
ENST00000217958.7:c.*347G= ENSP00000217958.3:n.*347G=
ENST00000372296.5:c.*493G= ENSP00000361370.1:n.*493G=
NM_002814.3:c.*347G= NP_002805.1:n.*347G=
NM_170750.2:c.*493G= NP_736606.1:n.*493G=
NM_002814.4:c.*347G= MANE Select NP_002805.1:n.*347G=
NM_170750.3:c.*493G= NP_736606.1:n.*493G=
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