Canonical Allele Identifier: CA2271700462

Gene: PSMD12

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350479A= , CM000679.2:g.67350479A=	GRCh38
NC_000017.10:g.65346595A= , CM000679.1:g.65346595A=	GRCh37
NC_000017.9:g.62777057A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.298-143T= MANE Select	ENSP00000348442.3:n.298-143T=
ENST00000356126.7:c.298-143T=	ENSP00000348442.3:n.298-143T=
ENST00000357146.4:c.238-143T=	ENSP00000349667.4:n.238-143T=
ENST00000579365.5:c.*348-143T=	ENSP00000463017.1:n.*348-143T=
ENST00000581618.1:n.535-143T=
ENST00000584008.5:c.*453-143T=	ENSP00000462525.1:n.*453-143T=
ENST00000584289.5:n.347-143T=
NM_001316341.1:c.121-143T=	NP_001303270.1:n.121-143T=
NM_002816.3:c.298-143T=	NP_002807.1:n.298-143T=
NM_002816.4:c.298-143T=	NP_002807.1:n.298-143T=
NM_174871.2:c.238-143T=	NP_777360.1:n.238-143T=
NM_174871.3:c.238-143T=	NP_777360.1:n.238-143T=
XM_011525048.1:c.121-143T=	XP_011523350.1:n.121-143T=
XM_011525049.1:c.121-143T=	XP_011523351.1:n.121-143T=
XM_011525050.1:c.298-143T=	XP_011523352.1:n.298-143T=
XM_024450842.1:c.385-143T=	XP_024306610.1:n.385-143T=
XM_024450843.1:c.121-143T=	XP_024306611.1:n.121-143T=
XR_001752571.2:n.377-143T=
NM_002816.5:c.298-143T= MANE Select	NP_002807.1:n.298-143T=
NM_001316341.2:c.121-143T=	NP_001303270.1:n.121-143T=
NM_174871.4:c.238-143T=	NP_777360.1:n.238-143T=