Canonical Allele Identifier: CA501602533

Gene: PSMD12

Linked Data

• MyVariant Identifiers: chr17:g.65346405G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350289G>T , CM000679.2:g.67350289G>T	GRCh38
NC_000017.10:g.65346405G>T , CM000679.1:g.65346405G>T	GRCh37
NC_000017.9:g.62776867G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.345C>A MANE Select	ENSP00000348442.3:p.Ile115=
ENST00000356126.7:c.345C>A	ENSP00000348442.3:p.Ile115=
ENST00000357146.4:c.285C>A	ENSP00000349667.4:p.Ile95=
ENST00000581618.1:n.582C>A
ENST00000584008.5:c.*500C>A	ENSP00000462525.1:n.*500C>A
ENST00000584289.5:n.394C>A
NM_001316341.1:c.168C>A	NP_001303270.1:p.Ile56=
NM_002816.3:c.345C>A	NP_002807.1:p.Ile115=
NM_002816.4:c.345C>A	NP_002807.1:p.Ile115=
NM_174871.2:c.285C>A	NP_777360.1:p.Ile95=
NM_174871.3:c.285C>A	NP_777360.1:p.Ile95=
XM_011525048.1:c.168C>A	XP_011523350.1:p.Ile56=
XM_011525049.1:c.168C>A	XP_011523351.1:p.Ile56=
XM_011525050.1:c.345C>A	XP_011523352.1:p.Ile115=
XM_024450842.1:c.432C>A	XP_024306610.1:p.Ile144=
XM_024450843.1:c.168C>A	XP_024306611.1:p.Ile56=
XR_001752571.2:n.424C>A
NM_002816.5:c.345C>A MANE Select	NP_002807.1:p.Ile115=
NM_001316341.2:c.168C>A	NP_001303270.1:p.Ile56=
NM_174871.4:c.285C>A	NP_777360.1:p.Ile95=