Canonical Allele Identifier: CA400805635

Gene: PSMD12

Linked Data

• MyVariant Identifiers: chr17:g.65346452C>T (hg19) ; chr17:g.67350336C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350336C>T , CM000679.2:g.67350336C>T	GRCh38
NC_000017.10:g.65346452C>T , CM000679.1:g.65346452C>T	GRCh37
NC_000017.9:g.62776914C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.298G>A MANE Select	ENSP00000348442.3:p.Ala100Thr
ENST00000356126.7:c.298G>A	ENSP00000348442.3:p.Ala100Thr
ENST00000357146.4:c.238G>A	ENSP00000349667.4:p.Ala80Thr
ENST00000579365.5:c.*348G>A	ENSP00000463017.1:n.*348G>A
ENST00000581618.1:n.535G>A
ENST00000584008.5:c.*453G>A	ENSP00000462525.1:n.*453G>A
ENST00000584289.5:n.347G>A
NM_001316341.1:c.121G>A	NP_001303270.1:p.Ala41Thr
NM_002816.3:c.298G>A	NP_002807.1:p.Ala100Thr
NM_002816.4:c.298G>A	NP_002807.1:p.Ala100Thr
NM_174871.2:c.238G>A	NP_777360.1:p.Ala80Thr
NM_174871.3:c.238G>A	NP_777360.1:p.Ala80Thr
XM_011525048.1:c.121G>A	XP_011523350.1:p.Ala41Thr
XM_011525049.1:c.121G>A	XP_011523351.1:p.Ala41Thr
XM_011525050.1:c.298G>A	XP_011523352.1:p.Ala100Thr
XM_024450842.1:c.385G>A	XP_024306610.1:p.Ala129Thr
XM_024450843.1:c.121G>A	XP_024306611.1:p.Ala41Thr
XR_001752571.2:n.377G>A
NM_002816.5:c.298G>A MANE Select	NP_002807.1:p.Ala100Thr
NM_001316341.2:c.121G>A	NP_001303270.1:p.Ala41Thr
NM_174871.4:c.238G>A	NP_777360.1:p.Ala80Thr