Canonical Allele Identifier: CA2466399769

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592655C= , CM000685.2:g.153592655C=	GRCh38
NC_000023.10:g.152858113C= , CM000685.1:g.152858113C=	GRCh37
NC_000023.9:g.152511307C=	NCBI36
NG_008393.2:g.11523G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.508G= MANE Select	ENSP00000461135.1:p.Ala170=
ENST00000429336.5:c.193+1892G=
ENST00000440428.5:c.508G=	ENSP00000402949.2:p.Ala170=
ENST00000482182.3:c.382G=	ENSP00000466345.1:p.Ala128=
ENST00000576892.7:c.508G=	ENSP00000461135.1:p.Ala170=
ENST00000614850.1:c.277+3349G=
ENST00000614851.4:c.329G=
ENST00000620088.4:c.*384G=	ENSP00000484108.1:n.*384G=
ENST00000621629.4:c.*384G=	ENSP00000478747.1:n.*384G=
ENST00000621817.1:c.*673G=	ENSP00000481634.1:n.*673G=
NM_001130997.2:c.508G=	NP_001124469.1:p.Ala170=
NM_152274.4:c.508G=	NP_689487.2:p.Ala170=
XM_005277920.3:c.478G=	XP_005277977.1:p.Ala160=
XM_005277921.3:c.478G=	XP_005277978.1:p.Ala160=
XM_011531213.1:c.382G=	XP_011529515.1:p.Ala128=
XM_011531214.1:c.382G=	XP_011529516.1:p.Ala128=
XM_011531215.1:c.382G=	XP_011529517.1:p.Ala128=
XM_005277920.4:c.478G=	XP_005277977.1:p.Ala160=
XM_005277921.4:c.478G=	XP_005277978.1:p.Ala160=
XM_011531214.2:c.382G=	XP_011529516.1:p.Ala128=
XM_011531215.2:c.382G=	XP_011529517.1:p.Ala128=
XR_002958810.1:n.2413G=
NM_152274.5:c.508G= MANE Select	NP_689487.2:p.Ala170=
NM_001130997.3:c.508G=	NP_001124469.1:p.Ala170=