Canonical Allele Identifier: CA2822885160
Gene: PSMD10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084541G>A , CM000685.2:g.108084541G>A GRCh38
NC_000023.10:g.107327771G>A , CM000685.1:g.107327771G>A GRCh37
NC_000023.9:g.107214427G>A NCBI36
NG_012521.1:g.12078C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*433C>T MANE Select ENSP00000217958.3:n.*433C>T
ENST00000217958.7:c.*433C>T ENSP00000217958.3:n.*433C>T
NM_002814.3:c.*433C>T NP_002805.1:n.*433C>T
NM_170750.2:c.*579C>T NP_736606.1:n.*579C>T
NM_002814.4:c.*433C>T MANE Select NP_002805.1:n.*433C>T
NM_170750.3:c.*579C>T NP_736606.1:n.*579C>T
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