Canonical Allele Identifier: CA2271700472
Gene: PSMD12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.67350506G= , CM000679.2:g.67350506G= GRCh38
NC_000017.10:g.65346622G= , CM000679.1:g.65346622G= GRCh37
NC_000017.9:g.62777084G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356126.8:c.298-170C= MANE Select ENSP00000348442.3:n.298-170C=
ENST00000356126.7:c.298-170C= ENSP00000348442.3:n.298-170C=
ENST00000357146.4:c.238-170C= ENSP00000349667.4:n.238-170C=
ENST00000579365.5:c.*348-170C= ENSP00000463017.1:n.*348-170C=
ENST00000581618.1:n.535-170C=
ENST00000584008.5:c.*453-170C= ENSP00000462525.1:n.*453-170C=
ENST00000584289.5:n.347-170C=
NM_001316341.1:c.121-170C= NP_001303270.1:n.121-170C=
NM_002816.3:c.298-170C= NP_002807.1:n.298-170C=
NM_002816.4:c.298-170C= NP_002807.1:n.298-170C=
NM_174871.2:c.238-170C= NP_777360.1:n.238-170C=
NM_174871.3:c.238-170C= NP_777360.1:n.238-170C=
XM_011525048.1:c.121-170C= XP_011523350.1:n.121-170C=
XM_011525049.1:c.121-170C= XP_011523351.1:n.121-170C=
XM_011525050.1:c.298-170C= XP_011523352.1:n.298-170C=
XM_024450842.1:c.385-170C= XP_024306610.1:n.385-170C=
XM_024450843.1:c.121-170C= XP_024306611.1:n.121-170C=
XR_001752571.2:n.377-170C=
NM_002816.5:c.298-170C= MANE Select NP_002807.1:n.298-170C=
NM_001316341.2:c.121-170C= NP_001303270.1:n.121-170C=
NM_174871.4:c.238-170C= NP_777360.1:n.238-170C=