Canonical Allele Identifier: CA413841763
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328332C>T (hg19) chrX:g.108085102C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085102C>T , CM000685.2:g.108085102C>T GRCh38
NC_000023.10:g.107328332C>T , CM000685.1:g.107328332C>T GRCh37
NC_000023.9:g.107214988C>T NCBI36
NG_012521.1:g.11517G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.553G>A MANE Select ENSP00000217958.3:p.Val185Met
ENST00000217958.7:c.553G>A ENSP00000217958.3:p.Val185Met
ENST00000340200.5:c.454G>A ENSP00000345963.5:p.Val152Met
ENST00000361815.9:c.*18G>A ENSP00000354906.5:n.*18G>A
ENST00000372295.5:c.430G>A ENSP00000361369.1:p.Val144Met
ENST00000372296.5:c.*18G>A ENSP00000361370.1:n.*18G>A
NM_002814.3:c.553G>A NP_002805.1:p.Val185Met
NM_170750.2:c.*18G>A NP_736606.1:n.*18G>A
NM_002814.4:c.553G>A MANE Select NP_002805.1:p.Val185Met
NM_170750.3:c.*18G>A NP_736606.1:n.*18G>A
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