Canonical Allele Identifier: CA2450520146
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084401G= , CM000685.2:g.108084401G= GRCh38
NC_000023.10:g.107327631G= , CM000685.1:g.107327631G= GRCh37
NC_000023.9:g.107214287G= NCBI36
NG_012521.1:g.12218C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*573C= MANE Select ENSP00000217958.3:n.*573C=
ENST00000217958.7:c.*573C= ENSP00000217958.3:n.*573C=
NM_002814.3:c.*573C= NP_002805.1:n.*573C=
NM_170750.2:c.*719C= NP_736606.1:n.*719C=
NM_002814.4:c.*573C= MANE Select NP_002805.1:n.*573C=
NM_170750.3:c.*719C= NP_736606.1:n.*719C=