Canonical Allele Identifier: CA413841647
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328280T>G (hg19) chrX:g.108085050T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085050T>G , CM000685.2:g.108085050T>G GRCh38
NC_000023.10:g.107328280T>G , CM000685.1:g.107328280T>G GRCh37
NC_000023.9:g.107214936T>G NCBI36
NG_012521.1:g.11569A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.605A>C MANE Select ENSP00000217958.3:p.Asn202Thr
ENST00000217958.7:c.605A>C ENSP00000217958.3:p.Asn202Thr
ENST00000340200.5:c.506A>C ENSP00000345963.5:p.Asn169Thr
ENST00000361815.9:c.*70A>C ENSP00000354906.5:n.*70A>C
ENST00000372295.5:c.482A>C ENSP00000361369.1:p.Asn161Thr
ENST00000372296.5:c.*70A>C ENSP00000361370.1:n.*70A>C
NM_002814.3:c.605A>C NP_002805.1:p.Asn202Thr
NM_170750.2:c.*70A>C NP_736606.1:n.*70A>C
NM_002814.4:c.605A>C MANE Select NP_002805.1:p.Asn202Thr
NM_170750.3:c.*70A>C NP_736606.1:n.*70A>C
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