Canonical Allele Identifier: CA643631641
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs1256742852

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084995del , CM000685.2:g.108084995del GRCh38
NC_000023.10:g.107328225del , CM000685.1:g.107328225del GRCh37
NC_000023.9:g.107214881del NCBI36
NG_012521.1:g.11624del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.660del MANE Select ENSP00000217958.3:p.Lys221ArgfsTer?
ENST00000217958.7:c.660del ENSP00000217958.3:p.Lys221ArgfsTer?
ENST00000340200.5:c.561del ENSP00000345963.5:p.Lys188ArgfsTer?
ENST00000361815.9:c.*125del ENSP00000354906.5:n.*125del
ENST00000372295.5:c.537del ENSP00000361369.1:p.Lys180ArgfsTer?
ENST00000372296.5:c.*125del ENSP00000361370.1:n.*125del
NM_002814.3:c.660del NP_002805.1:p.Lys221ArgfsTer?
NM_170750.2:c.*125del NP_736606.1:n.*125del
NM_002814.4:c.660del MANE Select NP_002805.1:p.Lys221ArgfsTer?
NM_170750.3:c.*125del NP_736606.1:n.*125del