Canonical Allele Identifier: CA517921151

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328213C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084983C>A , CM000685.2:g.108084983C>A	GRCh38
NC_000023.10:g.107328213C>A , CM000685.1:g.107328213C>A	GRCh37
NC_000023.9:g.107214869C>A	NCBI36
NG_012521.1:g.11636G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.672G>T MANE Select	ENSP00000217958.3:p.Val224=
ENST00000217958.7:c.672G>T	ENSP00000217958.3:p.Val224=
ENST00000340200.5:c.573G>T	ENSP00000345963.5:p.Val191=
ENST00000361815.9:c.*137G>T	ENSP00000354906.5:n.*137G>T
ENST00000372295.5:c.549G>T	ENSP00000361369.1:p.Val183=
ENST00000372296.5:c.*137G>T	ENSP00000361370.1:n.*137G>T
NM_002814.3:c.672G>T	NP_002805.1:p.Val224=
NM_170750.2:c.*137G>T	NP_736606.1:n.*137G>T
NM_002814.4:c.672G>T MANE Select	NP_002805.1:p.Val224=
NM_170750.3:c.*137G>T	NP_736606.1:n.*137G>T