Canonical Allele Identifier: CA333053222
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs1031647071
gnomAD v2: X-107327761-G-A
gnomAD v3: X-108084531-G-A
gnomAD v4: X-108084531-G-A
MyVariant Identifiers: chrX:g.107327761G>A (hg19) chrX:g.108084531G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084531G>A , CM000685.2:g.108084531G>A GRCh38
NC_000023.10:g.107327761G>A , CM000685.1:g.107327761G>A GRCh37
NC_000023.9:g.107214417G>A NCBI36
NG_012521.1:g.12088C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*443C>T MANE Select ENSP00000217958.3:n.*443C>T
ENST00000217958.7:c.*443C>T ENSP00000217958.3:n.*443C>T
NM_002814.3:c.*443C>T NP_002805.1:n.*443C>T
NM_170750.2:c.*589C>T NP_736606.1:n.*589C>T
NM_002814.4:c.*443C>T MANE Select NP_002805.1:n.*443C>T
NM_170750.3:c.*589C>T NP_736606.1:n.*589C>T
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