Canonical Allele Identifier: CA2466399761

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592625C= , CM000685.2:g.153592625C=	GRCh38
NC_000023.10:g.152858083C= , CM000685.1:g.152858083C=	GRCh37
NC_000023.9:g.152511277C=	NCBI36
NG_008393.2:g.11553G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.538G= MANE Select	ENSP00000461135.1:p.Gly180=
ENST00000429336.5:c.193+1922G=
ENST00000440428.5:c.538G=	ENSP00000402949.2:p.Gly180=
ENST00000482182.3:c.412G=	ENSP00000466345.1:p.Gly138=
ENST00000576892.7:c.538G=	ENSP00000461135.1:p.Gly180=
ENST00000614850.1:c.277+3379G=
ENST00000614851.4:c.359G=
ENST00000620088.4:c.*414G=	ENSP00000484108.1:n.*414G=
ENST00000621629.4:c.*414G=	ENSP00000478747.1:n.*414G=
ENST00000621817.1:c.*703G=	ENSP00000481634.1:n.*703G=
NM_001130997.2:c.538G=	NP_001124469.1:p.Gly180=
NM_152274.4:c.538G=	NP_689487.2:p.Gly180=
XM_005277920.3:c.508G=	XP_005277977.1:p.Gly170=
XM_005277921.3:c.508G=	XP_005277978.1:p.Gly170=
XM_011531213.1:c.412G=	XP_011529515.1:p.Gly138=
XM_011531214.1:c.412G=	XP_011529516.1:p.Gly138=
XM_011531215.1:c.412G=	XP_011529517.1:p.Gly138=
XM_005277920.4:c.508G=	XP_005277977.1:p.Gly170=
XM_005277921.4:c.508G=	XP_005277978.1:p.Gly170=
XM_011531214.2:c.412G=	XP_011529516.1:p.Gly138=
XM_011531215.2:c.412G=	XP_011529517.1:p.Gly138=
XR_002958810.1:n.2443G=
NM_152274.5:c.538G= MANE Select	NP_689487.2:p.Gly180=
NM_001130997.3:c.538G=	NP_001124469.1:p.Gly180=