Canonical Allele Identifier: CA14135397
Gene: CCDC33 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2930291

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74312493G>A , CM000677.2:g.74312493G>A GRCh38
NC_000015.9:g.74604834G>A , CM000677.1:g.74604834G>A GRCh37
NC_000015.8:g.72391887G>A NCBI36
NG_054754.1:g.114789G>A

Transcript Alleles

HGVS Amino-acid change
NM_025055.4:c.1290+16545G>A VV NP_079331.3:p.=
XM_005254692.1:c.1290+16545G>A XP_005254749.1:p.=
XM_006720697.2:c.1962+16545G>A XP_006720760.1:p.=
XM_011522085.1:c.1944+16545G>A XP_011520387.1:p.=
XM_011522086.1:c.1308+16545G>A XP_011520388.1:p.=
XM_011522087.1:c.1290+16545G>A XP_011520389.1:p.=
XM_011522088.1:c.1290+16545G>A XP_011520390.1:p.=
XM_011522089.1:c.402+16545G>A XP_011520391.1:p.=
XM_005254692.2:c.1290+16545G>A XP_005254749.1:p.=
XM_011522085.3:c.1944+16545G>A XP_011520387.1:p.=
XM_011522087.2:c.1290+16545G>A XP_011520389.1:p.=
XM_011522089.3:c.402+16545G>A XP_011520391.1:p.=
XM_017022623.1:c.1944+16545G>A XP_016878112.1:p.=
XM_017022624.1:c.1944+16545G>A XP_016878113.1:p.=
XM_017022625.1:c.1944+16545G>A XP_016878114.1:p.=
XM_017022626.2:c.1944+16545G>A XP_016878115.1:p.=
XM_017022627.1:c.1944+16545G>A XP_016878116.1:p.=
XM_017022628.1:c.1944+16545G>A XP_016878117.1:p.=
XR_001751400.1:n.2566+16545G>A
XR_001751401.1:n.2566+16545G>A
NM_025055.5:c.1290+16545G>A VV MANE Preferred NP_079331.3:p.=
ENST00000398814.7:c.1290+16545G>A ENSP00000381795.3:p.=
ENST00000558659.5:n.931+16545G>A