Canonical Allele Identifier: CA413841745
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328325T>C (hg19) chrX:g.108085095T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085095T>C , CM000685.2:g.108085095T>C GRCh38
NC_000023.10:g.107328325T>C , CM000685.1:g.107328325T>C GRCh37
NC_000023.9:g.107214981T>C NCBI36
NG_012521.1:g.11524A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.560A>G MANE Select ENSP00000217958.3:p.Glu187Gly
ENST00000217958.7:c.560A>G ENSP00000217958.3:p.Glu187Gly
ENST00000340200.5:c.461A>G ENSP00000345963.5:p.Glu154Gly
ENST00000361815.9:c.*25A>G ENSP00000354906.5:n.*25A>G
ENST00000372295.5:c.437A>G ENSP00000361369.1:p.Glu146Gly
ENST00000372296.5:c.*25A>G ENSP00000361370.1:n.*25A>G
NM_002814.3:c.560A>G NP_002805.1:p.Glu187Gly
NM_170750.2:c.*25A>G NP_736606.1:n.*25A>G
NM_002814.4:c.560A>G MANE Select NP_002805.1:p.Glu187Gly
NM_170750.3:c.*25A>G NP_736606.1:n.*25A>G
Search 100 bp 5'
Search 100 bp 3'