Canonical Allele Identifier: CA2450520142
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084382A= , CM000685.2:g.108084382A= GRCh38
NC_000023.10:g.107327612A= , CM000685.1:g.107327612A= GRCh37
NC_000023.9:g.107214268A= NCBI36
NG_012521.1:g.12237T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*592T= MANE Select ENSP00000217958.3:n.*592T=
ENST00000217958.7:c.*592T= ENSP00000217958.3:n.*592T=
NM_002814.3:c.*592T= NP_002805.1:n.*592T=
NM_170750.2:c.*738T= NP_736606.1:n.*738T=
NM_002814.4:c.*592T= MANE Select NP_002805.1:n.*592T=
NM_170750.3:c.*738T= NP_736606.1:n.*738T=