Canonical Allele Identifier: CA413841525

Gene: PSMD10

Linked Data

• MyVariant Identifiers: chrX:g.107328224T>C (hg19) ; chrX:g.108084994T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084994T>C , CM000685.2:g.108084994T>C	GRCh38
NC_000023.10:g.107328224T>C , CM000685.1:g.107328224T>C	GRCh37
NC_000023.9:g.107214880T>C	NCBI36
NG_012521.1:g.11625A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.661A>G MANE Select	ENSP00000217958.3:p.Lys221Glu
ENST00000217958.7:c.661A>G	ENSP00000217958.3:p.Lys221Glu
ENST00000340200.5:c.562A>G	ENSP00000345963.5:p.Lys188Glu
ENST00000361815.9:c.*126A>G	ENSP00000354906.5:n.*126A>G
ENST00000372295.5:c.538A>G	ENSP00000361369.1:p.Lys180Glu
ENST00000372296.5:c.*126A>G	ENSP00000361370.1:n.*126A>G
NM_002814.3:c.661A>G	NP_002805.1:p.Lys221Glu
NM_170750.2:c.*126A>G	NP_736606.1:n.*126A>G
NM_002814.4:c.661A>G MANE Select	NP_002805.1:p.Lys221Glu
NM_170750.3:c.*126A>G	NP_736606.1:n.*126A>G