Canonical Allele Identifier: CA413841759
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328331A>G (hg19) chrX:g.108085101A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085101A>G , CM000685.2:g.108085101A>G GRCh38
NC_000023.10:g.107328331A>G , CM000685.1:g.107328331A>G GRCh37
NC_000023.9:g.107214987A>G NCBI36
NG_012521.1:g.11518T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.554T>C MANE Select ENSP00000217958.3:p.Val185Ala
ENST00000217958.7:c.554T>C ENSP00000217958.3:p.Val185Ala
ENST00000340200.5:c.455T>C ENSP00000345963.5:p.Val152Ala
ENST00000361815.9:c.*19T>C ENSP00000354906.5:n.*19T>C
ENST00000372295.5:c.431T>C ENSP00000361369.1:p.Val144Ala
ENST00000372296.5:c.*19T>C ENSP00000361370.1:n.*19T>C
NM_002814.3:c.554T>C NP_002805.1:p.Val185Ala
NM_170750.2:c.*19T>C NP_736606.1:n.*19T>C
NM_002814.4:c.554T>C MANE Select NP_002805.1:p.Val185Ala
NM_170750.3:c.*19T>C NP_736606.1:n.*19T>C
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