Canonical Allele Identifier: CA413841688
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328296T>G (hg19) chrX:g.108085066T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085066T>G , CM000685.2:g.108085066T>G GRCh38
NC_000023.10:g.107328296T>G , CM000685.1:g.107328296T>G GRCh37
NC_000023.9:g.107214952T>G NCBI36
NG_012521.1:g.11553A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.589A>C MANE Select ENSP00000217958.3:p.Ser197Arg
ENST00000217958.7:c.589A>C ENSP00000217958.3:p.Ser197Arg
ENST00000340200.5:c.490A>C ENSP00000345963.5:p.Ser164Arg
ENST00000361815.9:c.*54A>C ENSP00000354906.5:n.*54A>C
ENST00000372295.5:c.466A>C ENSP00000361369.1:p.Ser156Arg
ENST00000372296.5:c.*54A>C ENSP00000361370.1:n.*54A>C
NM_002814.3:c.589A>C NP_002805.1:p.Ser197Arg
NM_170750.2:c.*54A>C NP_736606.1:n.*54A>C
NM_002814.4:c.589A>C MANE Select NP_002805.1:p.Ser197Arg
NM_170750.3:c.*54A>C NP_736606.1:n.*54A>C
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