Canonical Allele Identifier: CA413841533
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328228T>C (hg19) chrX:g.108084998T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084998T>C , CM000685.2:g.108084998T>C GRCh38
NC_000023.10:g.107328228T>C , CM000685.1:g.107328228T>C GRCh37
NC_000023.9:g.107214884T>C NCBI36
NG_012521.1:g.11621A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.657A>G MANE Select ENSP00000217958.3:p.Ile219Met
ENST00000217958.7:c.657A>G ENSP00000217958.3:p.Ile219Met
ENST00000340200.5:c.558A>G ENSP00000345963.5:p.Ile186Met
ENST00000361815.9:c.*122A>G ENSP00000354906.5:n.*122A>G
ENST00000372295.5:c.534A>G ENSP00000361369.1:p.Ile178Met
ENST00000372296.5:c.*122A>G ENSP00000361370.1:n.*122A>G
NM_002814.3:c.657A>G NP_002805.1:p.Ile219Met
NM_170750.2:c.*122A>G NP_736606.1:n.*122A>G
NM_002814.4:c.657A>G MANE Select NP_002805.1:p.Ile219Met
NM_170750.3:c.*122A>G NP_736606.1:n.*122A>G
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