Canonical Allele Identifier: CA413841612

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328266T>G (hg19) ; chrX:g.108085036T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108085036T>G , CM000685.2:g.108085036T>G	GRCh38
NC_000023.10:g.107328266T>G , CM000685.1:g.107328266T>G	GRCh37
NC_000023.9:g.107214922T>G	NCBI36
NG_012521.1:g.11583A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.619A>C MANE Select	ENSP00000217958.3:p.Thr207Pro
ENST00000217958.7:c.619A>C	ENSP00000217958.3:p.Thr207Pro
ENST00000340200.5:c.520A>C	ENSP00000345963.5:p.Thr174Pro
ENST00000361815.9:c.*84A>C	ENSP00000354906.5:n.*84A>C
ENST00000372295.5:c.496A>C	ENSP00000361369.1:p.Thr166Pro
ENST00000372296.5:c.*84A>C	ENSP00000361370.1:n.*84A>C
NM_002814.3:c.619A>C	NP_002805.1:p.Thr207Pro
NM_170750.2:c.*84A>C	NP_736606.1:n.*84A>C
NM_002814.4:c.619A>C MANE Select	NP_002805.1:p.Thr207Pro
NM_170750.3:c.*84A>C	NP_736606.1:n.*84A>C