Canonical Allele Identifier: CA517921154
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328222C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084992C>T , CM000685.2:g.108084992C>T GRCh38
NC_000023.10:g.107328222C>T , CM000685.1:g.107328222C>T GRCh37
NC_000023.9:g.107214878C>T NCBI36
NG_012521.1:g.11627G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.663G>A MANE Select ENSP00000217958.3:p.Lys221=
ENST00000217958.7:c.663G>A ENSP00000217958.3:p.Lys221=
ENST00000340200.5:c.564G>A ENSP00000345963.5:p.Lys188=
ENST00000361815.9:c.*128G>A ENSP00000354906.5:n.*128G>A
ENST00000372295.5:c.540G>A ENSP00000361369.1:p.Lys180=
ENST00000372296.5:c.*128G>A ENSP00000361370.1:n.*128G>A
NM_002814.3:c.663G>A NP_002805.1:p.Lys221=
NM_170750.2:c.*128G>A NP_736606.1:n.*128G>A
NM_002814.4:c.663G>A MANE Select NP_002805.1:p.Lys221=
NM_170750.3:c.*128G>A NP_736606.1:n.*128G>A
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