Canonical Allele Identifier: CA1136170066
Gene: PSMD10 HGNC NCBI

Linked Data

dbSNP Id: rs1705854370
gnomAD v3: X-108084351-C-T
gnomAD v4: X-108084351-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108084351C>T , CM000685.2:g.108084351C>T GRCh38
NC_000023.10:g.107327581C>T , CM000685.1:g.107327581C>T GRCh37
NC_000023.9:g.107214237C>T NCBI36
NG_012521.1:g.12268G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.*623G>A MANE Select ENSP00000217958.3:n.*623G>A
ENST00000217958.7:c.*623G>A ENSP00000217958.3:n.*623G>A
NM_002814.3:c.*623G>A NP_002805.1:n.*623G>A
NM_170750.2:c.*769G>A NP_736606.1:n.*769G>A
NM_002814.4:c.*623G>A MANE Select NP_002805.1:n.*623G>A
NM_170750.3:c.*769G>A NP_736606.1:n.*769G>A
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