Canonical Allele Identifier: CA2466401417

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153597180A= , CM000685.2:g.153597180A=	GRCh38
NC_000023.10:g.152862638A= , CM000685.1:g.152862638A=	GRCh37
NC_000023.9:g.152515832A=	NCBI36
NG_008393.2:g.6998T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.113-993T= MANE Select	ENSP00000461135.1:n.113-993T=
ENST00000440428.5:c.113-993T=	ENSP00000402949.2:n.113-993T=
ENST00000482182.3:c.-14-993T=	ENSP00000466345.1:n.-14-993T=
ENST00000576892.7:c.113-993T=	ENSP00000461135.1:n.113-993T=
ENST00000614850.1:c.94-993T=
ENST00000614851.4:c.67-993T=
ENST00000620088.4:c.109-993T=	ENSP00000484108.1:n.109-993T=
ENST00000621629.4:c.109-993T=	ENSP00000478747.1:n.109-993T=
ENST00000621817.1:c.*277+242T=	ENSP00000481634.1:n.*277+242T=
NM_001130997.2:c.113-993T=	NP_001124469.1:n.113-993T=
NM_152274.4:c.113-993T=	NP_689487.2:n.113-993T=
XM_005277920.3:c.113-993T=	XP_005277977.1:n.113-993T=
XM_005277921.3:c.113-993T=	XP_005277978.1:n.113-993T=
XM_011531213.1:c.-14-993T=	XP_011529515.1:n.-14-993T=
XM_011531214.1:c.-15+242T=	XP_011529516.1:n.-15+242T=
XM_011531215.1:c.-14-993T=	XP_011529517.1:n.-14-993T=
XM_005277920.4:c.113-993T=	XP_005277977.1:n.113-993T=
XM_005277921.4:c.113-993T=	XP_005277978.1:n.113-993T=
XM_011531214.2:c.-15+242T=	XP_011529516.1:n.-15+242T=
XM_011531215.2:c.-14-993T=	XP_011529517.1:n.-14-993T=
XR_002958810.1:n.205-993T=
NM_152274.5:c.113-993T= MANE Select	NP_689487.2:n.113-993T=
NM_001130997.3:c.113-993T=	NP_001124469.1:n.113-993T=