Canonical Allele Identifier: CA517921197
Gene: PSMD10 HGNC NCBI

Linked Data

gnomAD v4: X-108085052-C-T
MyVariant Identifiers: chrX:g.107328282C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085052C>T , CM000685.2:g.108085052C>T GRCh38
NC_000023.10:g.107328282C>T , CM000685.1:g.107328282C>T GRCh37
NC_000023.9:g.107214938C>T NCBI36
NG_012521.1:g.11567G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.603G>A MANE Select ENSP00000217958.3:p.Glu201=
ENST00000217958.7:c.603G>A ENSP00000217958.3:p.Glu201=
ENST00000340200.5:c.504G>A ENSP00000345963.5:p.Glu168=
ENST00000361815.9:c.*68G>A ENSP00000354906.5:n.*68G>A
ENST00000372295.5:c.480G>A ENSP00000361369.1:p.Glu160=
ENST00000372296.5:c.*68G>A ENSP00000361370.1:n.*68G>A
NM_002814.3:c.603G>A NP_002805.1:p.Glu201=
NM_170750.2:c.*68G>A NP_736606.1:n.*68G>A
NM_002814.4:c.603G>A MANE Select NP_002805.1:p.Glu201=
NM_170750.3:c.*68G>A NP_736606.1:n.*68G>A
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