Canonical Allele Identifier: CA869778581

Gene: PSMD10

Linked Data

• dbSNP Id: rs1411292971
• MyVariant Identifiers: chrX:g.107328029_107328035del (hg19) ; chrX:g.108084799_108084805del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084804_108084810del , CM000685.2:g.108084804_108084810del	GRCh38
NC_000023.10:g.107328034_107328040del , CM000685.1:g.107328034_107328040del	GRCh37
NC_000023.9:g.107214690_107214696del	NCBI36
NG_012521.1:g.11814_11820del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*169_*175del MANE Select	ENSP00000217958.3:n.*169_*175del
ENST00000217958.7:c.*169_*175del	ENSP00000217958.3:n.*169_*175del
ENST00000372295.5:c.*169_*175del	ENSP00000361369.1:n.*169_*175del
ENST00000372296.5:c.*315_*321del	ENSP00000361370.1:n.*315_*321del
NM_002814.3:c.*169_*175del	NP_002805.1:n.*169_*175del
NM_170750.2:c.*315_*321del	NP_736606.1:n.*315_*321del
NM_002814.4:c.*169_*175del MANE Select	NP_002805.1:n.*169_*175del
NM_170750.3:c.*315_*321del	NP_736606.1:n.*315_*321del