Canonical Allele Identifier: CA2639451166

Gene: PSMD12

Linked Data

• gnomAD v4: 17-67350371-A-ATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.67350373_67350374insTTTT , CM000679.2:g.67350373_67350374insTTTT	GRCh38
NC_000017.10:g.65346489_65346490insTTTT , CM000679.1:g.65346489_65346490insTTTT	GRCh37
NC_000017.9:g.62776951_62776952insTTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356126.8:c.298-36_298-35insAAAA MANE Select	ENSP00000348442.3:n.298-36_298-35insAAAA
ENST00000356126.7:c.298-36_298-35insAAAA	ENSP00000348442.3:n.298-36_298-35insAAAA
ENST00000357146.4:c.238-36_238-35insAAAA	ENSP00000349667.4:n.238-36_238-35insAAAA
ENST00000579365.5:c.*348-36_*348-35insAAAA	ENSP00000463017.1:n.*348-36_*348-35insAAAA
ENST00000581618.1:n.535-36_535-35insAAAA
ENST00000584008.5:c.*453-36_*453-35insAAAA	ENSP00000462525.1:n.*453-36_*453-35insAAAA
ENST00000584289.5:n.347-36_347-35insAAAA
NM_001316341.1:c.121-36_121-35insAAAA	NP_001303270.1:n.121-36_121-35insAAAA
NM_002816.3:c.298-36_298-35insAAAA	NP_002807.1:n.298-36_298-35insAAAA
NM_002816.4:c.298-36_298-35insAAAA	NP_002807.1:n.298-36_298-35insAAAA
NM_174871.2:c.238-36_238-35insAAAA	NP_777360.1:n.238-36_238-35insAAAA
NM_174871.3:c.238-36_238-35insAAAA	NP_777360.1:n.238-36_238-35insAAAA
XM_011525048.1:c.121-36_121-35insAAAA	XP_011523350.1:n.121-36_121-35insAAAA
XM_011525049.1:c.121-36_121-35insAAAA	XP_011523351.1:n.121-36_121-35insAAAA
XM_011525050.1:c.298-36_298-35insAAAA	XP_011523352.1:n.298-36_298-35insAAAA
XM_024450842.1:c.385-36_385-35insAAAA	XP_024306610.1:n.385-36_385-35insAAAA
XM_024450843.1:c.121-36_121-35insAAAA	XP_024306611.1:n.121-36_121-35insAAAA
XR_001752571.2:n.377-36_377-35insAAAA
NM_002816.5:c.298-36_298-35insAAAA MANE Select	NP_002807.1:n.298-36_298-35insAAAA
NM_001316341.2:c.121-36_121-35insAAAA	NP_001303270.1:n.121-36_121-35insAAAA
NM_174871.4:c.238-36_238-35insAAAA	NP_777360.1:n.238-36_238-35insAAAA