Canonical Allele Identifier: CA2271700392

Gene: PSMD12

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350314T= , CM000679.2:g.67350314T=	GRCh38
NC_000017.10:g.65346430T= , CM000679.1:g.65346430T=	GRCh37
NC_000017.9:g.62776892T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.320A= MANE Select	ENSP00000348442.3:p.Gln107=
ENST00000356126.7:c.320A=	ENSP00000348442.3:p.Gln107=
ENST00000357146.4:c.260A=	ENSP00000349667.4:p.Gln87=
ENST00000579365.5:c.*370A=	ENSP00000463017.1:n.*370A=
ENST00000581618.1:n.557A=
ENST00000584008.5:c.*475A=	ENSP00000462525.1:n.*475A=
ENST00000584289.5:n.369A=
NM_001316341.1:c.143A=	NP_001303270.1:p.Gln48=
NM_002816.3:c.320A=	NP_002807.1:p.Gln107=
NM_002816.4:c.320A=	NP_002807.1:p.Gln107=
NM_174871.2:c.260A=	NP_777360.1:p.Gln87=
NM_174871.3:c.260A=	NP_777360.1:p.Gln87=
XM_011525048.1:c.143A=	XP_011523350.1:p.Gln48=
XM_011525049.1:c.143A=	XP_011523351.1:p.Gln48=
XM_011525050.1:c.320A=	XP_011523352.1:p.Gln107=
XM_024450842.1:c.407A=	XP_024306610.1:p.Gln136=
XM_024450843.1:c.143A=	XP_024306611.1:p.Gln48=
XR_001752571.2:n.399A=
NM_002816.5:c.320A= MANE Select	NP_002807.1:p.Gln107=
NM_001316341.2:c.143A=	NP_001303270.1:p.Gln48=
NM_174871.4:c.260A=	NP_777360.1:p.Gln87=