Canonical Allele Identifier: CA413841727
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328317G>T (hg19) chrX:g.108085087G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085087G>T , CM000685.2:g.108085087G>T GRCh38
NC_000023.10:g.107328317G>T , CM000685.1:g.107328317G>T GRCh37
NC_000023.9:g.107214973G>T NCBI36
NG_012521.1:g.11532C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.568C>A MANE Select ENSP00000217958.3:p.Leu190Met
ENST00000217958.7:c.568C>A ENSP00000217958.3:p.Leu190Met
ENST00000340200.5:c.469C>A ENSP00000345963.5:p.Leu157Met
ENST00000361815.9:c.*33C>A ENSP00000354906.5:n.*33C>A
ENST00000372295.5:c.445C>A ENSP00000361369.1:p.Leu149Met
ENST00000372296.5:c.*33C>A ENSP00000361370.1:n.*33C>A
NM_002814.3:c.568C>A NP_002805.1:p.Leu190Met
NM_170750.2:c.*33C>A NP_736606.1:n.*33C>A
NM_002814.4:c.568C>A MANE Select NP_002805.1:p.Leu190Met
NM_170750.3:c.*33C>A NP_736606.1:n.*33C>A
Search 100 bp 5'
Search 100 bp 3'