Canonical Allele Identifier: CA643631495
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs1487993000
gnomAD v2: X-107327700-T-A
gnomAD v3: X-108084470-T-A
gnomAD v4: X-108084470-T-A
MyVariant Identifiers: chrX:g.107327700T>A (hg19) chrX:g.108084470T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084470T>A , CM000685.2:g.108084470T>A GRCh38
NC_000023.10:g.107327700T>A , CM000685.1:g.107327700T>A GRCh37
NC_000023.9:g.107214356T>A NCBI36
NG_012521.1:g.12149A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*504A>T MANE Select ENSP00000217958.3:n.*504A>T
ENST00000217958.7:c.*504A>T ENSP00000217958.3:n.*504A>T
NM_002814.3:c.*504A>T NP_002805.1:n.*504A>T
NM_170750.2:c.*650A>T NP_736606.1:n.*650A>T
NM_002814.4:c.*504A>T MANE Select NP_002805.1:n.*504A>T
NM_170750.3:c.*650A>T NP_736606.1:n.*650A>T
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