Canonical Allele Identifier: CA2450520178
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084523C= , CM000685.2:g.108084523C= GRCh38
NC_000023.10:g.107327753C= , CM000685.1:g.107327753C= GRCh37
NC_000023.9:g.107214409C= NCBI36
NG_012521.1:g.12096G=

Transcript Alleles

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