Canonical Allele Identifier: CA869778638

Gene: PSMD10

Linked Data

• dbSNP Id: rs1314971551
• MyVariant Identifiers: chrX:g.107328144A>C (hg19) ; chrX:g.108084914A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084914A>C , CM000685.2:g.108084914A>C	GRCh38
NC_000023.10:g.107328144A>C , CM000685.1:g.107328144A>C	GRCh37
NC_000023.9:g.107214800A>C	NCBI36
NG_012521.1:g.11705T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*60T>G MANE Select	ENSP00000217958.3:n.*60T>G
ENST00000217958.7:c.*60T>G	ENSP00000217958.3:n.*60T>G
ENST00000340200.5:c.642T>G	ENSP00000345963.5:n.642T>G
ENST00000361815.9:c.*206T>G	ENSP00000354906.5:n.*206T>G
ENST00000372295.5:c.*60T>G	ENSP00000361369.1:n.*60T>G
ENST00000372296.5:c.*206T>G	ENSP00000361370.1:n.*206T>G
NM_002814.3:c.*60T>G	NP_002805.1:n.*60T>G
NM_170750.2:c.*206T>G	NP_736606.1:n.*206T>G
NM_002814.4:c.*60T>G MANE Select	NP_002805.1:n.*60T>G
NM_170750.3:c.*206T>G	NP_736606.1:n.*206T>G