Canonical Allele Identifier: CA501602504

Gene: PSMD12

Linked Data

• MyVariant Identifiers: chr17:g.65346369A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350253A>C , CM000679.2:g.67350253A>C	GRCh38
NC_000017.10:g.65346369A>C , CM000679.1:g.65346369A>C	GRCh37
NC_000017.9:g.62776831A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.381T>G MANE Select	ENSP00000348442.3:p.Thr127=
ENST00000356126.7:c.381T>G	ENSP00000348442.3:p.Thr127=
ENST00000357146.4:c.321T>G	ENSP00000349667.4:p.Thr107=
ENST00000584008.5:c.*536T>G	ENSP00000462525.1:n.*536T>G
ENST00000584289.5:n.430T>G
NM_001316341.1:c.204T>G	NP_001303270.1:p.Thr68=
NM_002816.3:c.381T>G	NP_002807.1:p.Thr127=
NM_002816.4:c.381T>G	NP_002807.1:p.Thr127=
NM_174871.2:c.321T>G	NP_777360.1:p.Thr107=
NM_174871.3:c.321T>G	NP_777360.1:p.Thr107=
XM_011525048.1:c.204T>G	XP_011523350.1:p.Thr68=
XM_011525049.1:c.204T>G	XP_011523351.1:p.Thr68=
XM_011525050.1:c.381T>G	XP_011523352.1:p.Thr127=
XM_024450842.1:c.468T>G	XP_024306610.1:p.Thr156=
XM_024450843.1:c.204T>G	XP_024306611.1:p.Thr68=
XR_001752571.2:n.460T>G
NM_002816.5:c.381T>G MANE Select	NP_002807.1:p.Thr127=
NM_001316341.2:c.204T>G	NP_001303270.1:p.Thr68=
NM_174871.4:c.321T>G	NP_777360.1:p.Thr107=