Canonical Allele Identifier: CA2450520148

Gene: PSMD10

Linked Data

• dbSNP Id: rs2031471124

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084421T>C , CM000685.2:g.108084421T>C	GRCh38
NC_000023.10:g.107327651T>C , CM000685.1:g.107327651T>C	GRCh37
NC_000023.9:g.107214307T>C	NCBI36
NG_012521.1:g.12198A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*553A>G MANE Select	ENSP00000217958.3:n.*553A>G
ENST00000217958.7:c.*553A>G	ENSP00000217958.3:n.*553A>G
NM_002814.3:c.*553A>G	NP_002805.1:n.*553A>G
NM_170750.2:c.*699A>G	NP_736606.1:n.*699A>G
NM_002814.4:c.*553A>G MANE Select	NP_002805.1:n.*553A>G
NM_170750.3:c.*699A>G	NP_736606.1:n.*699A>G