Canonical Allele Identifier: CA8723776

Gene: PSMD12

Linked Data

• dbSNP Id: rs753998246
• ExAC: 17:65346422 T / C
• gnomAD v2: 17-65346422-T-C
• gnomAD v4: 17-67350306-T-C
• MyVariant Identifiers: chr17:g.65346422T>C (hg19) ; chr17:g.67350306T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350306T>C , CM000679.2:g.67350306T>C	GRCh38
NC_000017.10:g.65346422T>C , CM000679.1:g.65346422T>C	GRCh37
NC_000017.9:g.62776884T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.328A>G MANE Select	ENSP00000348442.3:p.Thr110Ala
ENST00000356126.7:c.328A>G	ENSP00000348442.3:p.Thr110Ala
ENST00000357146.4:c.268A>G	ENSP00000349667.4:p.Thr90Ala
ENST00000579365.5:c.*378A>G	ENSP00000463017.1:n.*378A>G
ENST00000581618.1:n.565A>G
ENST00000584008.5:c.*483A>G	ENSP00000462525.1:n.*483A>G
ENST00000584289.5:n.377A>G
NM_001316341.1:c.151A>G	NP_001303270.1:p.Thr51Ala
NM_002816.3:c.328A>G	NP_002807.1:p.Thr110Ala
NM_002816.4:c.328A>G	NP_002807.1:p.Thr110Ala
NM_174871.2:c.268A>G	NP_777360.1:p.Thr90Ala
NM_174871.3:c.268A>G	NP_777360.1:p.Thr90Ala
XM_011525048.1:c.151A>G	XP_011523350.1:p.Thr51Ala
XM_011525049.1:c.151A>G	XP_011523351.1:p.Thr51Ala
XM_011525050.1:c.328A>G	XP_011523352.1:p.Thr110Ala
XM_024450842.1:c.415A>G	XP_024306610.1:p.Thr139Ala
XM_024450843.1:c.151A>G	XP_024306611.1:p.Thr51Ala
XR_001752571.2:n.407A>G
NM_002816.5:c.328A>G MANE Select	NP_002807.1:p.Thr110Ala
NM_001316341.2:c.151A>G	NP_001303270.1:p.Thr51Ala
NM_174871.4:c.268A>G	NP_777360.1:p.Thr90Ala