Canonical Allele Identifier: CA2450520292

Gene: PSMD10

Linked Data

• dbSNP Id: rs2031477829

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084894G>A , CM000685.2:g.108084894G>A	GRCh38
NC_000023.10:g.107328124G>A , CM000685.1:g.107328124G>A	GRCh37
NC_000023.9:g.107214780G>A	NCBI36
NG_012521.1:g.11725C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000217958.8:c.*80C>T MANE Select	ENSP00000217958.3:n.*80C>T
ENST00000217958.7:c.*80C>T	ENSP00000217958.3:n.*80C>T
ENST00000340200.5:c.662C>T	ENSP00000345963.5:n.662C>T
ENST00000361815.9:c.*226C>T	ENSP00000354906.5:n.*226C>T
ENST00000372295.5:c.*80C>T	ENSP00000361369.1:n.*80C>T
ENST00000372296.5:c.*226C>T	ENSP00000361370.1:n.*226C>T
NM_002814.3:c.*80C>T	NP_002805.1:n.*80C>T
NM_170750.2:c.*226C>T	NP_736606.1:n.*226C>T
NM_002814.4:c.*80C>T MANE Select	NP_002805.1:n.*80C>T
NM_170750.3:c.*226C>T	NP_736606.1:n.*226C>T