Canonical Allele Identifier: CA413841515

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328220C>A (hg19) ; chrX:g.108084990C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084990C>A , CM000685.2:g.108084990C>A	GRCh38
NC_000023.10:g.107328220C>A , CM000685.1:g.107328220C>A	GRCh37
NC_000023.9:g.107214876C>A	NCBI36
NG_012521.1:g.11629G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.665G>T MANE Select	ENSP00000217958.3:p.Arg222Ile
ENST00000217958.7:c.665G>T	ENSP00000217958.3:p.Arg222Ile
ENST00000340200.5:c.566G>T	ENSP00000345963.5:p.Arg189Ile
ENST00000361815.9:c.*130G>T	ENSP00000354906.5:n.*130G>T
ENST00000372295.5:c.542G>T	ENSP00000361369.1:p.Arg181Ile
ENST00000372296.5:c.*130G>T	ENSP00000361370.1:n.*130G>T
NM_002814.3:c.665G>T	NP_002805.1:p.Arg222Ile
NM_170750.2:c.*130G>T	NP_736606.1:n.*130G>T
NM_002814.4:c.665G>T MANE Select	NP_002805.1:p.Arg222Ile
NM_170750.3:c.*130G>T	NP_736606.1:n.*130G>T