Canonical Allele Identifier: CA2450520263
Gene: PSMD10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084798_108084805delinsCAAGCTGT , CM000685.2:g.108084798_108084805delinsCAAGCTGT GRCh38
NC_000023.10:g.107328028_107328035delinsCAAGCTGT , CM000685.1:g.107328028_107328035delinsCAAGCTGT GRCh37
NC_000023.9:g.107214684_107214691delinsCAAGCTGT NCBI36
NG_012521.1:g.11814_11821delinsACAGCTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*169_*176delinsACAGCTTG MANE Select ENSP00000217958.3:n.*169_*176delinsACAGCTTG
ENST00000217958.7:c.*169_*176delinsACAGCTTG ENSP00000217958.3:n.*169_*176delinsACAGCTTG
ENST00000372295.5:c.*169_*176delinsACAGCTTG ENSP00000361369.1:n.*169_*176delinsACAGCTTG
ENST00000372296.5:c.*315_*322delinsACAGCTTG ENSP00000361370.1:n.*315_*322delinsACAGCTTG
NM_002814.3:c.*169_*176delinsACAGCTTG NP_002805.1:n.*169_*176delinsACAGCTTG
NM_170750.2:c.*315_*322delinsACAGCTTG NP_736606.1:n.*315_*322delinsACAGCTTG
NM_002814.4:c.*169_*176delinsACAGCTTG MANE Select NP_002805.1:n.*169_*176delinsACAGCTTG
NM_170750.3:c.*315_*322delinsACAGCTTG NP_736606.1:n.*315_*322delinsACAGCTTG
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