Canonical Allele Identifier: CA413841587
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328254C>T (hg19) chrX:g.108085024C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085024C>T , CM000685.2:g.108085024C>T GRCh38
NC_000023.10:g.107328254C>T , CM000685.1:g.107328254C>T GRCh37
NC_000023.9:g.107214910C>T NCBI36
NG_012521.1:g.11595G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.631G>A MANE Select ENSP00000217958.3:p.Val211Met
ENST00000217958.7:c.631G>A ENSP00000217958.3:p.Val211Met
ENST00000340200.5:c.532G>A ENSP00000345963.5:p.Val178Met
ENST00000361815.9:c.*96G>A ENSP00000354906.5:n.*96G>A
ENST00000372295.5:c.508G>A ENSP00000361369.1:p.Val170Met
ENST00000372296.5:c.*96G>A ENSP00000361370.1:n.*96G>A
NM_002814.3:c.631G>A NP_002805.1:p.Val211Met
NM_170750.2:c.*96G>A NP_736606.1:n.*96G>A
NM_002814.4:c.631G>A MANE Select NP_002805.1:p.Val211Met
NM_170750.3:c.*96G>A NP_736606.1:n.*96G>A
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