Canonical Allele Identifier: CA413841531
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328227G>C (hg19) chrX:g.108084997G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084997G>C , CM000685.2:g.108084997G>C GRCh38
NC_000023.10:g.107328227G>C , CM000685.1:g.107328227G>C GRCh37
NC_000023.9:g.107214883G>C NCBI36
NG_012521.1:g.11622C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.658C>G MANE Select ENSP00000217958.3:p.Leu220Val
ENST00000217958.7:c.658C>G ENSP00000217958.3:p.Leu220Val
ENST00000340200.5:c.559C>G ENSP00000345963.5:p.Leu187Val
ENST00000361815.9:c.*123C>G ENSP00000354906.5:n.*123C>G
ENST00000372295.5:c.535C>G ENSP00000361369.1:p.Leu179Val
ENST00000372296.5:c.*123C>G ENSP00000361370.1:n.*123C>G
NM_002814.3:c.658C>G NP_002805.1:p.Leu220Val
NM_170750.2:c.*123C>G NP_736606.1:n.*123C>G
NM_002814.4:c.658C>G MANE Select NP_002805.1:p.Leu220Val
NM_170750.3:c.*123C>G NP_736606.1:n.*123C>G
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