Canonical Allele Identifier: CA413841697
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328301C>T (hg19) chrX:g.108085071C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085071C>T , CM000685.2:g.108085071C>T GRCh38
NC_000023.10:g.107328301C>T , CM000685.1:g.107328301C>T GRCh37
NC_000023.9:g.107214957C>T NCBI36
NG_012521.1:g.11548G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.584G>A MANE Select ENSP00000217958.3:p.Gly195Glu
ENST00000217958.7:c.584G>A ENSP00000217958.3:p.Gly195Glu
ENST00000340200.5:c.485G>A ENSP00000345963.5:p.Gly162Glu
ENST00000361815.9:c.*49G>A ENSP00000354906.5:n.*49G>A
ENST00000372295.5:c.461G>A ENSP00000361369.1:p.Gly154Glu
ENST00000372296.5:c.*49G>A ENSP00000361370.1:n.*49G>A
NM_002814.3:c.584G>A NP_002805.1:p.Gly195Glu
NM_170750.2:c.*49G>A NP_736606.1:n.*49G>A
NM_002814.4:c.584G>A MANE Select NP_002805.1:p.Gly195Glu
NM_170750.3:c.*49G>A NP_736606.1:n.*49G>A
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Search 100 bp 3'