Canonical Allele Identifier: CA517921200

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328288G>A (hg19)
• PubMed: PMID:28263302

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085058G>A , CM000685.2:g.108085058G>A	GRCh38
NC_000023.10:g.107328288G>A , CM000685.1:g.107328288G>A	GRCh37
NC_000023.9:g.107214944G>A	NCBI36
NG_012521.1:g.11561C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.597C>T MANE Select	ENSP00000217958.3:p.Tyr199=
ENST00000217958.7:c.597C>T	ENSP00000217958.3:p.Tyr199=
ENST00000340200.5:c.498C>T	ENSP00000345963.5:p.Tyr166=
ENST00000361815.9:c.*62C>T	ENSP00000354906.5:n.*62C>T
ENST00000372295.5:c.474C>T	ENSP00000361369.1:p.Tyr158=
ENST00000372296.5:c.*62C>T	ENSP00000361370.1:n.*62C>T
NM_002814.3:c.597C>T	NP_002805.1:p.Tyr199=
NM_170750.2:c.*62C>T	NP_736606.1:n.*62C>T
NM_002814.4:c.597C>T MANE Select	NP_002805.1:p.Tyr199=
NM_170750.3:c.*62C>T	NP_736606.1:n.*62C>T