Canonical Allele Identifier: CA915952411

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153599059del , CM000685.2:g.153599059del	GRCh38
NG_008393.2:g.5121del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.17del MANE Select	ENSP00000461135.1:p.Gly6AlafsTer?
ENST00000440428.5:c.17del	ENSP00000402949.2:p.Gly6AlafsTer?
ENST00000482182.3:c.-15+850del	ENSP00000466345.1:n.-15+850del
ENST00000576892.7:c.17del	ENSP00000461135.1:p.Gly6AlafsTer?
ENST00000620088.4:c.17del	ENSP00000484108.1:p.Gly6AlafsTer?
ENST00000621629.4:c.17del	ENSP00000478747.1:p.Gly6AlafsTer?
ENST00000621817.1:c.17del	ENSP00000481634.1:p.Gly6AlafsTer?
NM_001130997.2:c.17del	NP_001124469.1:p.Gly6AlafsTer?
NM_152274.4:c.17del	NP_689487.2:p.Gly6AlafsTer?
XM_005277920.3:c.17del	XP_005277977.1:p.Gly6AlafsTer?
XM_005277921.3:c.17del	XP_005277978.1:p.Gly6AlafsTer?
XM_011531213.1:c.-106del	XP_011529515.1:n.-106del
XM_005277920.4:c.17del	XP_005277977.1:p.Gly6AlafsTer?
XM_005277921.4:c.17del	XP_005277978.1:p.Gly6AlafsTer?
XR_002958810.1:n.109del
NM_152274.5:c.17del MANE Select	NP_689487.2:p.Gly6AlafsTer?
NM_001130997.3:c.17del	NP_001124469.1:p.Gly6AlafsTer?