Canonical Allele Identifier: CA413841659
Gene: PSMD10 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.107328284C>T (hg19) chrX:g.108085054C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.108085054C>T , CM000685.2:g.108085054C>T GRCh38
NC_000023.10:g.107328284C>T , CM000685.1:g.107328284C>T GRCh37
NC_000023.9:g.107214940C>T NCBI36
NG_012521.1:g.11565G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217958.8:c.601G>A MANE Select ENSP00000217958.3:p.Glu201Lys
ENST00000217958.7:c.601G>A ENSP00000217958.3:p.Glu201Lys
ENST00000340200.5:c.502G>A ENSP00000345963.5:p.Glu168Lys
ENST00000361815.9:c.*66G>A ENSP00000354906.5:n.*66G>A
ENST00000372295.5:c.478G>A ENSP00000361369.1:p.Glu160Lys
ENST00000372296.5:c.*66G>A ENSP00000361370.1:n.*66G>A
NM_002814.3:c.601G>A NP_002805.1:p.Glu201Lys
NM_170750.2:c.*66G>A NP_736606.1:n.*66G>A
NM_002814.4:c.601G>A MANE Select NP_002805.1:p.Glu201Lys
NM_170750.3:c.*66G>A NP_736606.1:n.*66G>A
Search 100 bp 5'
Search 100 bp 3'