Canonical Allele Identifier: CA2271700396

Gene: PSMD12

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350329G= , CM000679.2:g.67350329G=	GRCh38
NC_000017.10:g.65346445G= , CM000679.1:g.65346445G=	GRCh37
NC_000017.9:g.62776907G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.305C= MANE Select	ENSP00000348442.3:p.Ala102=
ENST00000356126.7:c.305C=	ENSP00000348442.3:p.Ala102=
ENST00000357146.4:c.245C=	ENSP00000349667.4:p.Ala82=
ENST00000579365.5:c.*355C=	ENSP00000463017.1:n.*355C=
ENST00000581618.1:n.542C=
ENST00000584008.5:c.*460C=	ENSP00000462525.1:n.*460C=
ENST00000584289.5:n.354C=
NM_001316341.1:c.128C=	NP_001303270.1:p.Ala43=
NM_002816.3:c.305C=	NP_002807.1:p.Ala102=
NM_002816.4:c.305C=	NP_002807.1:p.Ala102=
NM_174871.2:c.245C=	NP_777360.1:p.Ala82=
NM_174871.3:c.245C=	NP_777360.1:p.Ala82=
XM_011525048.1:c.128C=	XP_011523350.1:p.Ala43=
XM_011525049.1:c.128C=	XP_011523351.1:p.Ala43=
XM_011525050.1:c.305C=	XP_011523352.1:p.Ala102=
XM_024450842.1:c.392C=	XP_024306610.1:p.Ala131=
XM_024450843.1:c.128C=	XP_024306611.1:p.Ala43=
XR_001752571.2:n.384C=
NM_002816.5:c.305C= MANE Select	NP_002807.1:p.Ala102=
NM_001316341.2:c.128C=	NP_001303270.1:p.Ala43=
NM_174871.4:c.245C=	NP_777360.1:p.Ala82=