Canonical Allele Identifier: CA413841681
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328294A>C (hg19) chrX:g.108085064A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085064A>C , CM000685.2:g.108085064A>C GRCh38
NC_000023.10:g.107328294A>C , CM000685.1:g.107328294A>C GRCh37
NC_000023.9:g.107214950A>C NCBI36
NG_012521.1:g.11555T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.591T>G MANE Select ENSP00000217958.3:p.Ser197Arg
ENST00000217958.7:c.591T>G ENSP00000217958.3:p.Ser197Arg
ENST00000340200.5:c.492T>G ENSP00000345963.5:p.Ser164Arg
ENST00000361815.9:c.*56T>G ENSP00000354906.5:n.*56T>G
ENST00000372295.5:c.468T>G ENSP00000361369.1:p.Ser156Arg
ENST00000372296.5:c.*56T>G ENSP00000361370.1:n.*56T>G
NM_002814.3:c.591T>G NP_002805.1:p.Ser197Arg
NM_170750.2:c.*56T>G NP_736606.1:n.*56T>G
NM_002814.4:c.591T>G MANE Select NP_002805.1:p.Ser197Arg
NM_170750.3:c.*56T>G NP_736606.1:n.*56T>G
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