Canonical Allele Identifier: CA2450520252
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084768_108084770delinsAAT , CM000685.2:g.108084768_108084770delinsAAT GRCh38
NC_000023.10:g.107327998_107328000delinsAAT , CM000685.1:g.107327998_107328000delinsAAT GRCh37
NC_000023.9:g.107214654_107214656delinsAAT NCBI36
NG_012521.1:g.11849_11851delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*204_*206delinsATT MANE Select ENSP00000217958.3:n.*204_*206delinsATT
ENST00000217958.7:c.*204_*206delinsATT ENSP00000217958.3:n.*204_*206delinsATT
ENST00000372296.5:c.*350_*352delinsATT ENSP00000361370.1:n.*350_*352delinsATT
NM_002814.3:c.*204_*206delinsATT NP_002805.1:n.*204_*206delinsATT
NM_170750.2:c.*350_*352delinsATT NP_736606.1:n.*350_*352delinsATT
NM_002814.4:c.*204_*206delinsATT MANE Select NP_002805.1:n.*204_*206delinsATT
NM_170750.3:c.*350_*352delinsATT NP_736606.1:n.*350_*352delinsATT