Canonical Allele Identifier: CA2694424296
Gene: PSMD10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084995_108084998del , CM000685.2:g.108084995_108084998del GRCh38
NC_000023.10:g.107328225_107328228del , CM000685.1:g.107328225_107328228del GRCh37
NC_000023.9:g.107214881_107214884del NCBI36
NG_012521.1:g.11622_11625del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.658_661del MANE Select ENSP00000217958.3:p.Leu220ArgfsTer?
ENST00000217958.7:c.658_661del ENSP00000217958.3:p.Leu220ArgfsTer?
ENST00000340200.5:c.559_562del ENSP00000345963.5:p.Leu187ArgfsTer?
ENST00000361815.9:c.*123_*126del ENSP00000354906.5:n.*123_*126del
ENST00000372295.5:c.535_538del ENSP00000361369.1:p.Leu179ArgfsTer?
ENST00000372296.5:c.*123_*126del ENSP00000361370.1:n.*123_*126del
NM_002814.3:c.658_661del NP_002805.1:p.Leu220ArgfsTer?
NM_170750.2:c.*123_*126del NP_736606.1:n.*123_*126del
NM_002814.4:c.658_661del MANE Select NP_002805.1:p.Leu220ArgfsTer?
NM_170750.3:c.*123_*126del NP_736606.1:n.*123_*126del