Canonical Allele Identifier: CA400805511
Gene: PSMD12 HGNC NCBI

Linked Data

dbSNP Id: rs1416789554

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.67350283G>T , CM000679.2:g.67350283G>T GRCh38
NC_000017.10:g.65346399G>T , CM000679.1:g.65346399G>T GRCh37
NC_000017.9:g.62776861G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356126.8:c.351C>A MANE Select ENSP00000348442.3:p.Asp117Glu
ENST00000356126.7:c.351C>A ENSP00000348442.3:p.Asp117Glu
ENST00000357146.4:c.291C>A ENSP00000349667.4:p.Asp97Glu
ENST00000581618.1:n.588C>A
ENST00000584008.5:c.*506C>A ENSP00000462525.1:n.*506C>A
ENST00000584289.5:n.400C>A
NM_001316341.1:c.174C>A NP_001303270.1:p.Asp58Glu
NM_002816.3:c.351C>A NP_002807.1:p.Asp117Glu
NM_002816.4:c.351C>A NP_002807.1:p.Asp117Glu
NM_174871.2:c.291C>A NP_777360.1:p.Asp97Glu
NM_174871.3:c.291C>A NP_777360.1:p.Asp97Glu
XM_011525048.1:c.174C>A XP_011523350.1:p.Asp58Glu
XM_011525049.1:c.174C>A XP_011523351.1:p.Asp58Glu
XM_011525050.1:c.351C>A XP_011523352.1:p.Asp117Glu
XM_024450842.1:c.438C>A XP_024306610.1:p.Asp146Glu
XM_024450843.1:c.174C>A XP_024306611.1:p.Asp58Glu
XR_001752571.2:n.430C>A
NM_002816.5:c.351C>A MANE Select NP_002807.1:p.Asp117Glu
NM_001316341.2:c.174C>A NP_001303270.1:p.Asp58Glu
NM_174871.4:c.291C>A NP_777360.1:p.Asp97Glu