Canonical Allele Identifier: CA2450520140
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084349T= , CM000685.2:g.108084349T= GRCh38
NC_000023.10:g.107327579T= , CM000685.1:g.107327579T= GRCh37
NC_000023.9:g.107214235T= NCBI36
NG_012521.1:g.12270A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*625A= MANE Select ENSP00000217958.3:n.*625A=
ENST00000217958.7:c.*625A= ENSP00000217958.3:n.*625A=
NM_002814.3:c.*625A= NP_002805.1:n.*625A=
NM_170750.2:c.*771A= NP_736606.1:n.*771A=
NM_002814.4:c.*625A= MANE Select NP_002805.1:n.*625A=
NM_170750.3:c.*771A= NP_736606.1:n.*771A=