Canonical Allele Identifier: CA2271700358

Gene: PSMD12

Linked Data

• dbSNP Id: rs2042004556
• gnomAD v4: 17-67350199-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350199C>T , CM000679.2:g.67350199C>T	GRCh38
NC_000017.10:g.65346315C>T , CM000679.1:g.65346315C>T	GRCh37
NC_000017.9:g.62776777C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.405+30G>A MANE Select	ENSP00000348442.3:n.405+30G>A
ENST00000356126.7:c.405+30G>A	ENSP00000348442.3:n.405+30G>A
ENST00000357146.4:c.345+30G>A	ENSP00000349667.4:n.345+30G>A
ENST00000584008.5:c.*560+30G>A	ENSP00000462525.1:n.*560+30G>A
ENST00000584289.5:n.454+30G>A
NM_001316341.1:c.228+30G>A	NP_001303270.1:n.228+30G>A
NM_002816.3:c.405+30G>A	NP_002807.1:n.405+30G>A
NM_002816.4:c.405+30G>A	NP_002807.1:n.405+30G>A
NM_174871.2:c.345+30G>A	NP_777360.1:n.345+30G>A
NM_174871.3:c.345+30G>A	NP_777360.1:n.345+30G>A
XM_011525048.1:c.228+30G>A	XP_011523350.1:n.228+30G>A
XM_011525049.1:c.228+30G>A	XP_011523351.1:n.228+30G>A
XM_011525050.1:c.405+30G>A	XP_011523352.1:n.405+30G>A
XM_024450842.1:c.492+30G>A	XP_024306610.1:n.492+30G>A
XM_024450843.1:c.228+30G>A	XP_024306611.1:n.228+30G>A
XR_001752571.2:n.484+30G>A
NM_002816.5:c.405+30G>A MANE Select	NP_002807.1:n.405+30G>A
NM_001316341.2:c.228+30G>A	NP_001303270.1:n.228+30G>A
NM_174871.4:c.345+30G>A	NP_777360.1:n.345+30G>A