Canonical Allele Identifier: CA413841806

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328350C>G (hg19) ; chrX:g.108085120C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085120C>G , CM000685.2:g.108085120C>G	GRCh38
NC_000023.10:g.107328350C>G , CM000685.1:g.107328350C>G	GRCh37
NC_000023.9:g.107215006C>G	NCBI36
NG_012521.1:g.11499G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.535G>C MANE Select	ENSP00000217958.3:p.Ala179Pro
ENST00000217958.7:c.535G>C	ENSP00000217958.3:p.Ala179Pro
ENST00000340200.5:c.436G>C	ENSP00000345963.5:p.Ala146Pro
ENST00000361815.9:c.456G>C	ENSP00000354906.5:p.Ter152Tyr
ENST00000372295.5:c.412G>C	ENSP00000361369.1:p.Ala138Pro
ENST00000372296.5:c.333G>C	ENSP00000361370.1:p.Ter111Tyr
NM_002814.3:c.535G>C	NP_002805.1:p.Ala179Pro
NM_170750.2:c.456G>C	NP_736606.1:p.Ter152Tyr
NM_002814.4:c.535G>C MANE Select	NP_002805.1:p.Ala179Pro
NM_170750.3:c.456G>C	NP_736606.1:p.Ter152Tyr