Canonical Allele Identifier: CA2466399732

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592551T= , CM000685.2:g.153592551T=	GRCh38
NC_000023.10:g.152858009T= , CM000685.1:g.152858009T=	GRCh37
NC_000023.9:g.152511203T=	NCBI36
NG_008393.2:g.11627A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000576892.8:c.612A= MANE Select	ENSP00000461135.1:p.Gly204=
ENST00000429336.5:c.193+1996A=
ENST00000440428.5:c.612A=	ENSP00000402949.2:p.Gly204=
ENST00000576892.7:c.612A=	ENSP00000461135.1:p.Gly204=
ENST00000614850.1:c.277+3453A=
ENST00000614851.4:c.433A=
ENST00000620088.4:c.*488A=	ENSP00000484108.1:n.*488A=
ENST00000621629.4:c.*488A=	ENSP00000478747.1:n.*488A=
NM_001130997.2:c.612A=	NP_001124469.1:p.Gly204=
NM_152274.4:c.612A=	NP_689487.2:p.Gly204=
XM_005277920.3:c.582A=	XP_005277977.1:p.Gly194=
XM_005277921.3:c.582A=	XP_005277978.1:p.Gly194=
XM_011531213.1:c.486A=	XP_011529515.1:p.Gly162=
XM_011531214.1:c.486A=	XP_011529516.1:p.Gly162=
XM_011531215.1:c.486A=	XP_011529517.1:p.Gly162=
XM_005277920.4:c.582A=	XP_005277977.1:p.Gly194=
XM_005277921.4:c.582A=	XP_005277978.1:p.Gly194=
XM_011531214.2:c.486A=	XP_011529516.1:p.Gly162=
XM_011531215.2:c.486A=	XP_011529517.1:p.Gly162=
XR_002958810.1:n.2517A=
NM_152274.5:c.612A= MANE Select	NP_689487.2:p.Gly204=
NM_001130997.3:c.612A=	NP_001124469.1:p.Gly204=