Canonical Allele Identifier: CA2450520323
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085017T= , CM000685.2:g.108085017T= GRCh38
NC_000023.10:g.107328247T= , CM000685.1:g.107328247T= GRCh37
NC_000023.9:g.107214903T= NCBI36
NG_012521.1:g.11602A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.638A= MANE Select ENSP00000217958.3:p.Lys213=
ENST00000217958.7:c.638A= ENSP00000217958.3:p.Lys213=
ENST00000340200.5:c.539A= ENSP00000345963.5:p.Lys180=
ENST00000361815.9:c.*103A= ENSP00000354906.5:n.*103A=
ENST00000372295.5:c.515A= ENSP00000361369.1:p.Lys172=
ENST00000372296.5:c.*103A= ENSP00000361370.1:n.*103A=
NM_002814.3:c.638A= NP_002805.1:p.Lys213=
NM_170750.2:c.*103A= NP_736606.1:n.*103A=
NM_002814.4:c.638A= MANE Select NP_002805.1:p.Lys213=
NM_170750.3:c.*103A= NP_736606.1:n.*103A=