Canonical Allele Identifier: CA413841534

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328229A>C (hg19) ; chrX:g.108084999A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084999A>C , CM000685.2:g.108084999A>C	GRCh38
NC_000023.10:g.107328229A>C , CM000685.1:g.107328229A>C	GRCh37
NC_000023.9:g.107214885A>C	NCBI36
NG_012521.1:g.11620T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.656T>G MANE Select	ENSP00000217958.3:p.Ile219Arg
ENST00000217958.7:c.656T>G	ENSP00000217958.3:p.Ile219Arg
ENST00000340200.5:c.557T>G	ENSP00000345963.5:p.Ile186Arg
ENST00000361815.9:c.*121T>G	ENSP00000354906.5:n.*121T>G
ENST00000372295.5:c.533T>G	ENSP00000361369.1:p.Ile178Arg
ENST00000372296.5:c.*121T>G	ENSP00000361370.1:n.*121T>G
NM_002814.3:c.656T>G	NP_002805.1:p.Ile219Arg
NM_170750.2:c.*121T>G	NP_736606.1:n.*121T>G
NM_002814.4:c.656T>G MANE Select	NP_002805.1:p.Ile219Arg
NM_170750.3:c.*121T>G	NP_736606.1:n.*121T>G