Canonical Allele Identifier: CA413841673
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328290A>T (hg19) chrX:g.108085060A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085060A>T , CM000685.2:g.108085060A>T GRCh38
NC_000023.10:g.107328290A>T , CM000685.1:g.107328290A>T GRCh37
NC_000023.9:g.107214946A>T NCBI36
NG_012521.1:g.11559T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.595T>A MANE Select ENSP00000217958.3:p.Tyr199Asn
ENST00000217958.7:c.595T>A ENSP00000217958.3:p.Tyr199Asn
ENST00000340200.5:c.496T>A ENSP00000345963.5:p.Tyr166Asn
ENST00000361815.9:c.*60T>A ENSP00000354906.5:n.*60T>A
ENST00000372295.5:c.472T>A ENSP00000361369.1:p.Tyr158Asn
ENST00000372296.5:c.*60T>A ENSP00000361370.1:n.*60T>A
NM_002814.3:c.595T>A NP_002805.1:p.Tyr199Asn
NM_170750.2:c.*60T>A NP_736606.1:n.*60T>A
NM_002814.4:c.595T>A MANE Select NP_002805.1:p.Tyr199Asn
NM_170750.3:c.*60T>A NP_736606.1:n.*60T>A
Search 100 bp 5'
Search 100 bp 3'