Canonical Allele Identifier: CA2187596257

Gene: CCDC33

Linked Data

• dbSNP Id: rs9783698

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74256432G>T , CM000677.2:g.74256432G>T	GRCh38
NC_000015.9:g.74548773G>T , CM000677.1:g.74548773G>T	GRCh37
NC_000015.8:g.72335826G>T	NCBI36
NG_054754.1:g.58728G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635913.2:c.840-6008G>T	ENSP00000490425.2:n.840-6008G>T
ENST00000398814.8:c.186-6008G>T MANE Select	ENSP00000381795.3:n.186-6008G>T
ENST00000398814.7:c.186-6008G>T	ENSP00000381795.3:n.186-6008G>T
NM_025055.4:c.186-6008G>T	NP_079331.3:n.186-6008G>T
XM_005254692.1:c.186-6008G>T	XP_005254749.1:n.186-6008G>T
XM_006720697.2:c.858-6008G>T	XP_006720760.1:n.858-6008G>T
XM_011522085.1:c.840-6008G>T	XP_011520387.1:n.840-6008G>T
XM_011522086.1:c.204-6008G>T	XP_011520388.1:n.204-6008G>T
XM_011522087.1:c.186-6008G>T	XP_011520389.1:n.186-6008G>T
XM_011522088.1:c.186-6008G>T	XP_011520390.1:n.186-6008G>T
XM_005254692.2:c.186-6008G>T	XP_005254749.1:n.186-6008G>T
XM_011522085.3:c.840-6008G>T	XP_011520387.1:n.840-6008G>T
XM_011522087.2:c.186-6008G>T	XP_011520389.1:n.186-6008G>T
XM_017022623.1:c.840-6008G>T	XP_016878112.1:n.840-6008G>T
XM_017022624.1:c.840-6008G>T	XP_016878113.1:n.840-6008G>T
XM_017022625.1:c.840-6008G>T	XP_016878114.1:n.840-6008G>T
XM_017022626.2:c.840-6008G>T	XP_016878115.1:n.840-6008G>T
XM_017022627.1:c.840-6008G>T	XP_016878116.1:n.840-6008G>T
XM_017022628.1:c.840-6008G>T	XP_016878117.1:n.840-6008G>T
XM_017022630.1:c.840-6008G>T	XP_016878119.1:n.840-6008G>T
XM_017022631.1:c.840-6008G>T	XP_016878120.1:n.840-6008G>T
XM_017022633.1:c.840-6008G>T	XP_016878122.1:n.840-6008G>T
XR_001751400.1:n.1462-6008G>T
XR_001751401.1:n.1462-6008G>T
NM_025055.5:c.186-6008G>T MANE Select	NP_079331.3:n.186-6008G>T