Canonical Allele Identifier: CA643631640
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs1226764606
gnomAD v2: X-107328173-A-G
gnomAD v3: X-108084943-A-G
gnomAD v4: X-108084943-A-G
MyVariant Identifiers: chrX:g.107328173A>G (hg19) chrX:g.108084943A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084943A>G , CM000685.2:g.108084943A>G GRCh38
NC_000023.10:g.107328173A>G , CM000685.1:g.107328173A>G GRCh37
NC_000023.9:g.107214829A>G NCBI36
NG_012521.1:g.11676T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*31T>C MANE Select ENSP00000217958.3:n.*31T>C
ENST00000217958.7:c.*31T>C ENSP00000217958.3:n.*31T>C
ENST00000340200.5:c.613T>C ENSP00000345963.5:n.613T>C
ENST00000361815.9:c.*177T>C ENSP00000354906.5:n.*177T>C
ENST00000372295.5:c.*31T>C ENSP00000361369.1:n.*31T>C
ENST00000372296.5:c.*177T>C ENSP00000361370.1:n.*177T>C
NM_002814.3:c.*31T>C NP_002805.1:n.*31T>C
NM_170750.2:c.*177T>C NP_736606.1:n.*177T>C
NM_002814.4:c.*31T>C MANE Select NP_002805.1:n.*31T>C
NM_170750.3:c.*177T>C NP_736606.1:n.*177T>C
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