Canonical Allele Identifier: CA517921196

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328279A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085049A>G , CM000685.2:g.108085049A>G	GRCh38
NC_000023.10:g.107328279A>G , CM000685.1:g.107328279A>G	GRCh37
NC_000023.9:g.107214935A>G	NCBI36
NG_012521.1:g.11570T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.606T>C MANE Select	ENSP00000217958.3:p.Asn202=
ENST00000217958.7:c.606T>C	ENSP00000217958.3:p.Asn202=
ENST00000340200.5:c.507T>C	ENSP00000345963.5:p.Asn169=
ENST00000361815.9:c.*71T>C	ENSP00000354906.5:n.*71T>C
ENST00000372295.5:c.483T>C	ENSP00000361369.1:p.Asn161=
ENST00000372296.5:c.*71T>C	ENSP00000361370.1:n.*71T>C
NM_002814.3:c.606T>C	NP_002805.1:p.Asn202=
NM_170750.2:c.*71T>C	NP_736606.1:n.*71T>C
NM_002814.4:c.606T>C MANE Select	NP_002805.1:p.Asn202=
NM_170750.3:c.*71T>C	NP_736606.1:n.*71T>C