Canonical Allele Identifier: CA2466399684

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592387T= , CM000685.2:g.153592387T=	GRCh38
NC_000023.10:g.152857845T= , CM000685.1:g.152857845T=	GRCh37
NC_000023.9:g.152511039T=	NCBI36
NG_008393.2:g.11791A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.657+119A= MANE Select	ENSP00000461135.1:n.657+119A=
ENST00000429336.5:c.193+2160A=
ENST00000440428.5:c.657+119A=	ENSP00000402949.2:n.657+119A=
ENST00000576892.7:c.657+119A=	ENSP00000461135.1:n.657+119A=
ENST00000614850.1:c.277+3617A=
ENST00000614851.4:c.478+119A=
ENST00000620088.4:c.*533+119A=	ENSP00000484108.1:n.*533+119A=
ENST00000621629.4:c.*533+119A=	ENSP00000478747.1:n.*533+119A=
NM_001130997.2:c.657+119A=	NP_001124469.1:n.657+119A=
NM_152274.4:c.657+119A=	NP_689487.2:n.657+119A=
XM_005277920.3:c.627+119A=	XP_005277977.1:n.627+119A=
XM_005277921.3:c.627+119A=	XP_005277978.1:n.627+119A=
XM_011531213.1:c.531+119A=	XP_011529515.1:n.531+119A=
XM_011531214.1:c.531+119A=	XP_011529516.1:n.531+119A=
XM_011531215.1:c.531+119A=	XP_011529517.1:n.531+119A=
XM_005277920.4:c.627+119A=	XP_005277977.1:n.627+119A=
XM_005277921.4:c.627+119A=	XP_005277978.1:n.627+119A=
XM_011531214.2:c.531+119A=	XP_011529516.1:n.531+119A=
XM_011531215.2:c.531+119A=	XP_011529517.1:n.531+119A=
XR_002958810.1:n.2562+119A=
NM_152274.5:c.657+119A= MANE Select	NP_689487.2:n.657+119A=
NM_001130997.3:c.657+119A=	NP_001124469.1:n.657+119A=