Canonical Allele Identifier: CA2450520137
Gene: PSMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084341G= , CM000685.2:g.108084341G= GRCh38
NC_000023.10:g.107327571G= , CM000685.1:g.107327571G= GRCh37
NC_000023.9:g.107214227G= NCBI36
NG_012521.1:g.12278C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*633C= MANE Select ENSP00000217958.3:n.*633C=
ENST00000217958.7:c.*633C= ENSP00000217958.3:n.*633C=
NM_002814.3:c.*633C= NP_002805.1:n.*633C=
NM_170750.2:c.*779C= NP_736606.1:n.*779C=
NM_002814.4:c.*633C= MANE Select NP_002805.1:n.*633C=
NM_170750.3:c.*779C= NP_736606.1:n.*779C=