Canonical Allele Identifier: CA2501359872

Gene: PSMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108084935_108084936insCT , CM000685.2:g.108084935_108084936insCT	GRCh38
NC_000023.10:g.107328165_107328166insCT , CM000685.1:g.107328165_107328166insCT	GRCh37
NC_000023.9:g.107214821_107214822insCT	NCBI36
NG_012521.1:g.11683_11684insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217958.8:c.*38_*39insAG MANE Select	ENSP00000217958.3:n.*38_*39insAG
ENST00000217958.7:c.*38_*39insAG	ENSP00000217958.3:n.*38_*39insAG
ENST00000340200.5:c.620_621insAG	ENSP00000345963.5:n.620_621insAG
ENST00000361815.9:c.*184_*185insAG	ENSP00000354906.5:n.*184_*185insAG
ENST00000372295.5:c.*38_*39insAG	ENSP00000361369.1:n.*38_*39insAG
ENST00000372296.5:c.*184_*185insAG	ENSP00000361370.1:n.*184_*185insAG
NM_002814.3:c.*38_*39insAG	NP_002805.1:n.*38_*39insAG
NM_170750.2:c.*184_*185insAG	NP_736606.1:n.*184_*185insAG
NM_002814.4:c.*38_*39insAG MANE Select	NP_002805.1:n.*38_*39insAG
NM_170750.3:c.*184_*185insAG	NP_736606.1:n.*184_*185insAG