Canonical Allele Identifier: CA2466399711

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592479G= , CM000685.2:g.153592479G=	GRCh38
NC_000023.10:g.152857937G= , CM000685.1:g.152857937G=	GRCh37
NC_000023.9:g.152511131G=	NCBI36
NG_008393.2:g.11699C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.657+27C= MANE Select	ENSP00000461135.1:n.657+27C=
ENST00000429336.5:c.193+2068C=
ENST00000440428.5:c.657+27C=	ENSP00000402949.2:n.657+27C=
ENST00000576892.7:c.657+27C=	ENSP00000461135.1:n.657+27C=
ENST00000614850.1:c.277+3525C=
ENST00000614851.4:c.478+27C=
ENST00000620088.4:c.*533+27C=	ENSP00000484108.1:n.*533+27C=
ENST00000621629.4:c.*533+27C=	ENSP00000478747.1:n.*533+27C=
NM_001130997.2:c.657+27C=	NP_001124469.1:n.657+27C=
NM_152274.4:c.657+27C=	NP_689487.2:n.657+27C=
XM_005277920.3:c.627+27C=	XP_005277977.1:n.627+27C=
XM_005277921.3:c.627+27C=	XP_005277978.1:n.627+27C=
XM_011531213.1:c.531+27C=	XP_011529515.1:n.531+27C=
XM_011531214.1:c.531+27C=	XP_011529516.1:n.531+27C=
XM_011531215.1:c.531+27C=	XP_011529517.1:n.531+27C=
XM_005277920.4:c.627+27C=	XP_005277977.1:n.627+27C=
XM_005277921.4:c.627+27C=	XP_005277978.1:n.627+27C=
XM_011531214.2:c.531+27C=	XP_011529516.1:n.531+27C=
XM_011531215.2:c.531+27C=	XP_011529517.1:n.531+27C=
XR_002958810.1:n.2562+27C=
NM_152274.5:c.657+27C= MANE Select	NP_689487.2:n.657+27C=
NM_001130997.3:c.657+27C=	NP_001124469.1:n.657+27C=