Canonical Allele Identifier: CA643631492
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs1490010256
gnomAD v2: X-107327656-A-G
MyVariant Identifiers: chrX:g.107327656A>G (hg19) chrX:g.108084426A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084426A>G , CM000685.2:g.108084426A>G GRCh38
NC_000023.10:g.107327656A>G , CM000685.1:g.107327656A>G GRCh37
NC_000023.9:g.107214312A>G NCBI36
NG_012521.1:g.12193T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*548T>C MANE Select ENSP00000217958.3:n.*548T>C
ENST00000217958.7:c.*548T>C ENSP00000217958.3:n.*548T>C
NM_002814.3:c.*548T>C NP_002805.1:n.*548T>C
NM_170750.2:c.*694T>C NP_736606.1:n.*694T>C
NM_002814.4:c.*548T>C MANE Select NP_002805.1:n.*548T>C
NM_170750.3:c.*694T>C NP_736606.1:n.*694T>C
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