Canonical Allele Identifier: CA2450520288
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084890T= , CM000685.2:g.108084890T= GRCh38
NC_000023.10:g.107328120T= , CM000685.1:g.107328120T= GRCh37
NC_000023.9:g.107214776T= NCBI36
NG_012521.1:g.11729A=

Transcript Alleles

HGVS Amino-acid change
ENST00000217958.8:c.*84A= MANE Select ENSP00000217958.3:n.*84A=
ENST00000217958.7:c.*84A= ENSP00000217958.3:n.*84A=
ENST00000340200.5:c.666A= ENSP00000345963.5:n.666A=
ENST00000361815.9:c.*230A= ENSP00000354906.5:n.*230A=
ENST00000372295.5:c.*84A= ENSP00000361369.1:n.*84A=
ENST00000372296.5:c.*230A= ENSP00000361370.1:n.*230A=
NM_002814.3:c.*84A= NP_002805.1:n.*84A=
NM_170750.2:c.*230A= NP_736606.1:n.*230A=
NM_002814.4:c.*84A= MANE Select NP_002805.1:n.*84A=
NM_170750.3:c.*230A= NP_736606.1:n.*230A=