Canonical Allele Identifier: CA517921195
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328276T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085046T>C , CM000685.2:g.108085046T>C GRCh38
NC_000023.10:g.107328276T>C , CM000685.1:g.107328276T>C GRCh37
NC_000023.9:g.107214932T>C NCBI36
NG_012521.1:g.11573A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.609A>G MANE Select ENSP00000217958.3:p.Lys203=
ENST00000217958.7:c.609A>G ENSP00000217958.3:p.Lys203=
ENST00000340200.5:c.510A>G ENSP00000345963.5:p.Lys170=
ENST00000361815.9:c.*74A>G ENSP00000354906.5:n.*74A>G
ENST00000372295.5:c.486A>G ENSP00000361369.1:p.Lys162=
ENST00000372296.5:c.*74A>G ENSP00000361370.1:n.*74A>G
NM_002814.3:c.609A>G NP_002805.1:p.Lys203=
NM_170750.2:c.*74A>G NP_736606.1:n.*74A>G
NM_002814.4:c.609A>G MANE Select NP_002805.1:p.Lys203=
NM_170750.3:c.*74A>G NP_736606.1:n.*74A>G
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