Canonical Allele Identifier: CA413841817

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328354G>C (hg19) ; chrX:g.108085124G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085124G>C , CM000685.2:g.108085124G>C	GRCh38
NC_000023.10:g.107328354G>C , CM000685.1:g.107328354G>C	GRCh37
NC_000023.9:g.107215010G>C	NCBI36
NG_012521.1:g.11495C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.531C>G MANE Select	ENSP00000217958.3:p.His177Gln
ENST00000217958.7:c.531C>G	ENSP00000217958.3:p.His177Gln
ENST00000340200.5:c.432C>G	ENSP00000345963.5:p.His144Gln
ENST00000361815.9:c.452C>G	ENSP00000354906.5:p.Thr151Ser
ENST00000372295.5:c.408C>G	ENSP00000361369.1:p.His136Gln
ENST00000372296.5:c.329C>G	ENSP00000361370.1:p.Thr110Ser
NM_002814.3:c.531C>G	NP_002805.1:p.His177Gln
NM_170750.2:c.452C>G	NP_736606.1:p.Thr151Ser
NM_002814.4:c.531C>G MANE Select	NP_002805.1:p.His177Gln
NM_170750.3:c.452C>G	NP_736606.1:p.Thr151Ser