Canonical Allele Identifier: CA501602526

Gene: PSMD12

Linked Data

• MyVariant Identifiers: chr17:g.65346396A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350280A>T , CM000679.2:g.67350280A>T	GRCh38
NC_000017.10:g.65346396A>T , CM000679.1:g.65346396A>T	GRCh37
NC_000017.9:g.62776858A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.354T>A MANE Select	ENSP00000348442.3:p.Leu118=
ENST00000356126.7:c.354T>A	ENSP00000348442.3:p.Leu118=
ENST00000357146.4:c.294T>A	ENSP00000349667.4:p.Leu98=
ENST00000581618.1:n.591T>A
ENST00000584008.5:c.*509T>A	ENSP00000462525.1:n.*509T>A
ENST00000584289.5:n.403T>A
NM_001316341.1:c.177T>A	NP_001303270.1:p.Leu59=
NM_002816.3:c.354T>A	NP_002807.1:p.Leu118=
NM_002816.4:c.354T>A	NP_002807.1:p.Leu118=
NM_174871.2:c.294T>A	NP_777360.1:p.Leu98=
NM_174871.3:c.294T>A	NP_777360.1:p.Leu98=
XM_011525048.1:c.177T>A	XP_011523350.1:p.Leu59=
XM_011525049.1:c.177T>A	XP_011523351.1:p.Leu59=
XM_011525050.1:c.354T>A	XP_011523352.1:p.Leu118=
XM_024450842.1:c.441T>A	XP_024306610.1:p.Leu147=
XM_024450843.1:c.177T>A	XP_024306611.1:p.Leu59=
XR_001752571.2:n.433T>A
NM_002816.5:c.354T>A MANE Select	NP_002807.1:p.Leu118=
NM_001316341.2:c.177T>A	NP_001303270.1:p.Leu59=
NM_174871.4:c.294T>A	NP_777360.1:p.Leu98=