Canonical Allele Identifier: CA2450520260
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs2031476483
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084792G>A , CM000685.2:g.108084792G>A GRCh38
NC_000023.10:g.107328022G>A , CM000685.1:g.107328022G>A GRCh37
NC_000023.9:g.107214678G>A NCBI36
NG_012521.1:g.11827C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*182C>T MANE Select ENSP00000217958.3:n.*182C>T
ENST00000217958.7:c.*182C>T ENSP00000217958.3:n.*182C>T
ENST00000372295.5:c.*182C>T ENSP00000361369.1:n.*182C>T
ENST00000372296.5:c.*328C>T ENSP00000361370.1:n.*328C>T
NM_002814.3:c.*182C>T NP_002805.1:n.*182C>T
NM_170750.2:c.*328C>T NP_736606.1:n.*328C>T
NM_002814.4:c.*182C>T MANE Select NP_002805.1:n.*182C>T
NM_170750.3:c.*328C>T NP_736606.1:n.*328C>T
Search 100 bp 5'
Search 100 bp 3'