Canonical Allele Identifier: CA869778546
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs1347997691
gnomAD v3: X-108084681-G-A
gnomAD v4: X-108084681-G-A
MyVariant Identifiers: chrX:g.107327911G>A (hg19) chrX:g.108084681G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084681G>A , CM000685.2:g.108084681G>A GRCh38
NC_000023.10:g.107327911G>A , CM000685.1:g.107327911G>A GRCh37
NC_000023.9:g.107214567G>A NCBI36
NG_012521.1:g.11938C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*293C>T MANE Select ENSP00000217958.3:n.*293C>T
ENST00000217958.7:c.*293C>T ENSP00000217958.3:n.*293C>T
ENST00000372296.5:c.*439C>T ENSP00000361370.1:n.*439C>T
NM_002814.3:c.*293C>T NP_002805.1:n.*293C>T
NM_170750.2:c.*439C>T NP_736606.1:n.*439C>T
NM_002814.4:c.*293C>T MANE Select NP_002805.1:n.*293C>T
NM_170750.3:c.*439C>T NP_736606.1:n.*439C>T
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