Canonical Allele Identifier: CA2534078568

Gene: CCDC33

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74312515_74312516insA , CM000677.2:g.74312515_74312516insA	GRCh38
NC_000015.9:g.74604856_74604857insA , CM000677.1:g.74604856_74604857insA	GRCh37
NC_000015.8:g.72391909_72391910insA	NCBI36
NG_054754.1:g.114811_114812insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000635913.2:c.1944+16567_1944+16568insA	ENSP00000490425.2:n.1944+16567_1944+16568...
ENST00000398814.8:c.1290+16567_1290+16568insA MANE Select	ENSP00000381795.3:n.1290+16567_1290+16568...
ENST00000398814.7:c.1290+16567_1290+16568insA	ENSP00000381795.3:n.1290+16567_1290+16568...
ENST00000558659.5:c.931+16567_931+16568insA
NM_025055.4:c.1290+16567_1290+16568insA	NP_079331.3:n.1290+16567_1290+16568insA
XM_005254692.1:c.1290+16567_1290+16568insA	XP_005254749.1:n.1290+16567_1290+16568ins...
XM_006720697.2:c.1962+16567_1962+16568insA	XP_006720760.1:n.1962+16567_1962+16568ins...
XM_011522085.1:c.1944+16567_1944+16568insA	XP_011520387.1:n.1944+16567_1944+16568ins...
XM_011522086.1:c.1308+16567_1308+16568insA	XP_011520388.1:n.1308+16567_1308+16568ins...
XM_011522087.1:c.1290+16567_1290+16568insA	XP_011520389.1:n.1290+16567_1290+16568ins...
XM_011522088.1:c.1290+16567_1290+16568insA	XP_011520390.1:n.1290+16567_1290+16568ins...
XM_011522089.1:c.402+16567_402+16568insA	XP_011520391.1:n.402+16567_402+16568insA
XM_005254692.2:c.1290+16567_1290+16568insA	XP_005254749.1:n.1290+16567_1290+16568ins...
XM_011522085.3:c.1944+16567_1944+16568insA	XP_011520387.1:n.1944+16567_1944+16568ins...
XM_011522087.2:c.1290+16567_1290+16568insA	XP_011520389.1:n.1290+16567_1290+16568ins...
XM_011522089.3:c.402+16567_402+16568insA	XP_011520391.1:n.402+16567_402+16568insA
XM_017022623.1:c.1944+16567_1944+16568insA	XP_016878112.1:n.1944+16567_1944+16568ins...
XM_017022624.1:c.1944+16567_1944+16568insA	XP_016878113.1:n.1944+16567_1944+16568ins...
XM_017022625.1:c.1944+16567_1944+16568insA	XP_016878114.1:n.1944+16567_1944+16568ins...
XM_017022626.2:c.1944+16567_1944+16568insA	XP_016878115.1:n.1944+16567_1944+16568ins...
XM_017022627.1:c.1944+16567_1944+16568insA	XP_016878116.1:n.1944+16567_1944+16568ins...
XM_017022628.1:c.1944+16567_1944+16568insA	XP_016878117.1:n.1944+16567_1944+16568ins...
XR_001751400.1:n.2566+16567_2566+16568insA
XR_001751401.1:n.2566+16567_2566+16568insA
NM_025055.5:c.1290+16567_1290+16568insA MANE Select	NP_079331.3:n.1290+16567_1290+16568insA