Canonical Allele Identifier: CA413841822

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328356G>A (hg19) ; chrX:g.108085126G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085126G>A , CM000685.2:g.108085126G>A	GRCh38
NC_000023.10:g.107328356G>A , CM000685.1:g.107328356G>A	GRCh37
NC_000023.9:g.107215012G>A	NCBI36
NG_012521.1:g.11493C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.529C>T MANE Select	ENSP00000217958.3:p.His177Tyr
ENST00000217958.7:c.529C>T	ENSP00000217958.3:p.His177Tyr
ENST00000340200.5:c.430C>T	ENSP00000345963.5:p.His144Tyr
ENST00000361815.9:c.450C>T	ENSP00000354906.5:p.Asp150=
ENST00000372295.5:c.406C>T	ENSP00000361369.1:p.His136Tyr
ENST00000372296.5:c.327C>T	ENSP00000361370.1:p.Asp109=
NM_002814.3:c.529C>T	NP_002805.1:p.His177Tyr
NM_170750.2:c.450C>T	NP_736606.1:p.Asp150=
NM_002814.4:c.529C>T MANE Select	NP_002805.1:p.His177Tyr
NM_170750.3:c.450C>T	NP_736606.1:p.Asp150=