Canonical Allele Identifier: CA2271700385

Gene: PSMD12

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350285C= , CM000679.2:g.67350285C=	GRCh38
NC_000017.10:g.65346401C= , CM000679.1:g.65346401C=	GRCh37
NC_000017.9:g.62776863C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.349G= MANE Select	ENSP00000348442.3:p.Asp117=
ENST00000356126.7:c.349G=	ENSP00000348442.3:p.Asp117=
ENST00000357146.4:c.289G=	ENSP00000349667.4:p.Asp97=
ENST00000581618.1:n.586G=
ENST00000584008.5:c.*504G=	ENSP00000462525.1:n.*504G=
ENST00000584289.5:n.398G=
NM_001316341.1:c.172G=	NP_001303270.1:p.Asp58=
NM_002816.3:c.349G=	NP_002807.1:p.Asp117=
NM_002816.4:c.349G=	NP_002807.1:p.Asp117=
NM_174871.2:c.289G=	NP_777360.1:p.Asp97=
NM_174871.3:c.289G=	NP_777360.1:p.Asp97=
XM_011525048.1:c.172G=	XP_011523350.1:p.Asp58=
XM_011525049.1:c.172G=	XP_011523351.1:p.Asp58=
XM_011525050.1:c.349G=	XP_011523352.1:p.Asp117=
XM_024450842.1:c.436G=	XP_024306610.1:p.Asp146=
XM_024450843.1:c.172G=	XP_024306611.1:p.Asp58=
XR_001752571.2:n.428G=
NM_002816.5:c.349G= MANE Select	NP_002807.1:p.Asp117=
NM_001316341.2:c.172G=	NP_001303270.1:p.Asp58=
NM_174871.4:c.289G=	NP_777360.1:p.Asp97=