Canonical Allele Identifier: CA2450520177
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084523_108084524delinsCG , CM000685.2:g.108084523_108084524delinsCG GRCh38
NC_000023.10:g.107327753_107327754delinsCG , CM000685.1:g.107327753_107327754delinsCG GRCh37
NC_000023.9:g.107214409_107214410delinsCG NCBI36
NG_012521.1:g.12095_12096delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*450_*451delinsCG MANE Select ENSP00000217958.3:n.*450_*451delinsCG
ENST00000217958.7:c.*450_*451delinsCG ENSP00000217958.3:n.*450_*451delinsCG
NM_002814.3:c.*450_*451delinsCG NP_002805.1:n.*450_*451delinsCG
NM_170750.2:c.*596_*597delinsCG NP_736606.1:n.*596_*597delinsCG
NM_002814.4:c.*450_*451delinsCG MANE Select NP_002805.1:n.*450_*451delinsCG
NM_170750.3:c.*596_*597delinsCG NP_736606.1:n.*596_*597delinsCG