Canonical Allele Identifier: CA2466399725

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592535C= , CM000685.2:g.153592535C=	GRCh38
NC_000023.10:g.152857993C= , CM000685.1:g.152857993C=	GRCh37
NC_000023.9:g.152511187C=	NCBI36
NG_008393.2:g.11643G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.628G= MANE Select	ENSP00000461135.1:p.Glu210=
ENST00000429336.5:c.193+2012G=
ENST00000440428.5:c.628G=	ENSP00000402949.2:p.Glu210=
ENST00000576892.7:c.628G=	ENSP00000461135.1:p.Glu210=
ENST00000614850.1:c.277+3469G=
ENST00000614851.4:c.449G=
ENST00000620088.4:c.*504G=	ENSP00000484108.1:n.*504G=
ENST00000621629.4:c.*504G=	ENSP00000478747.1:n.*504G=
NM_001130997.2:c.628G=	NP_001124469.1:p.Glu210=
NM_152274.4:c.628G=	NP_689487.2:p.Glu210=
XM_005277920.3:c.598G=	XP_005277977.1:p.Glu200=
XM_005277921.3:c.598G=	XP_005277978.1:p.Glu200=
XM_011531213.1:c.502G=	XP_011529515.1:p.Glu168=
XM_011531214.1:c.502G=	XP_011529516.1:p.Glu168=
XM_011531215.1:c.502G=	XP_011529517.1:p.Glu168=
XM_005277920.4:c.598G=	XP_005277977.1:p.Glu200=
XM_005277921.4:c.598G=	XP_005277978.1:p.Glu200=
XM_011531214.2:c.502G=	XP_011529516.1:p.Glu168=
XM_011531215.2:c.502G=	XP_011529517.1:p.Glu168=
XR_002958810.1:n.2533G=
NM_152274.5:c.628G= MANE Select	NP_689487.2:p.Glu210=
NM_001130997.3:c.628G=	NP_001124469.1:p.Glu210=