Canonical Allele Identifier: CA400805618
Gene: PSMD12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.67350327T>G , CM000679.2:g.67350327T>G GRCh38
NC_000017.10:g.65346443T>G , CM000679.1:g.65346443T>G GRCh37
NC_000017.9:g.62776905T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356126.8:c.307A>C MANE Select ENSP00000348442.3:p.Lys103Gln
ENST00000356126.7:c.307A>C ENSP00000348442.3:p.Lys103Gln
ENST00000357146.4:c.247A>C ENSP00000349667.4:p.Lys83Gln
ENST00000579365.5:c.*357A>C ENSP00000463017.1:n.*357A>C
ENST00000581618.1:n.544A>C
ENST00000584008.5:c.*462A>C ENSP00000462525.1:n.*462A>C
ENST00000584289.5:n.356A>C
NM_001316341.1:c.130A>C NP_001303270.1:p.Lys44Gln
NM_002816.3:c.307A>C NP_002807.1:p.Lys103Gln
NM_002816.4:c.307A>C NP_002807.1:p.Lys103Gln
NM_174871.2:c.247A>C NP_777360.1:p.Lys83Gln
NM_174871.3:c.247A>C NP_777360.1:p.Lys83Gln
XM_011525048.1:c.130A>C XP_011523350.1:p.Lys44Gln
XM_011525049.1:c.130A>C XP_011523351.1:p.Lys44Gln
XM_011525050.1:c.307A>C XP_011523352.1:p.Lys103Gln
XM_024450842.1:c.394A>C XP_024306610.1:p.Lys132Gln
XM_024450843.1:c.130A>C XP_024306611.1:p.Lys44Gln
XR_001752571.2:n.386A>C
NM_002816.5:c.307A>C MANE Select NP_002807.1:p.Lys103Gln
NM_001316341.2:c.130A>C NP_001303270.1:p.Lys44Gln
NM_174871.4:c.247A>C NP_777360.1:p.Lys83Gln