Canonical Allele Identifier: CA2450520144
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084397A= , CM000685.2:g.108084397A= GRCh38
NC_000023.10:g.107327627A= , CM000685.1:g.107327627A= GRCh37
NC_000023.9:g.107214283A= NCBI36
NG_012521.1:g.12222T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*577T= MANE Select ENSP00000217958.3:n.*577T=
ENST00000217958.7:c.*577T= ENSP00000217958.3:n.*577T=
NM_002814.3:c.*577T= NP_002805.1:n.*577T=
NM_170750.2:c.*723T= NP_736606.1:n.*723T=
NM_002814.4:c.*577T= MANE Select NP_002805.1:n.*577T=
NM_170750.3:c.*723T= NP_736606.1:n.*723T=