Canonical Allele Identifier: CA869778398
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs1410420834
gnomAD v3: X-108084397-A-T
gnomAD v4: X-108084397-A-T
MyVariant Identifiers: chrX:g.107327627A>T (hg19) chrX:g.108084397A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084397A>T , CM000685.2:g.108084397A>T GRCh38
NC_000023.10:g.107327627A>T , CM000685.1:g.107327627A>T GRCh37
NC_000023.9:g.107214283A>T NCBI36
NG_012521.1:g.12222T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*577T>A MANE Select ENSP00000217958.3:n.*577T>A
ENST00000217958.7:c.*577T>A ENSP00000217958.3:n.*577T>A
NM_002814.3:c.*577T>A NP_002805.1:n.*577T>A
NM_170750.2:c.*723T>A NP_736606.1:n.*723T>A
NM_002814.4:c.*577T>A MANE Select NP_002805.1:n.*577T>A
NM_170750.3:c.*723T>A NP_736606.1:n.*723T>A
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