Canonical Allele Identifier: CA2466399758

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592620C= , CM000685.2:g.153592620C=	GRCh38
NC_000023.10:g.152858078C= , CM000685.1:g.152858078C=	GRCh37
NC_000023.9:g.152511272C=	NCBI36
NG_008393.2:g.11558G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.543G= MANE Select	ENSP00000461135.1:p.Ala181=
ENST00000429336.5:c.193+1927G=
ENST00000440428.5:c.543G=	ENSP00000402949.2:p.Ala181=
ENST00000482182.3:c.417G=	ENSP00000466345.1:p.Ala139=
ENST00000576892.7:c.543G=	ENSP00000461135.1:p.Ala181=
ENST00000614850.1:c.277+3384G=
ENST00000614851.4:c.364G=
ENST00000620088.4:c.*419G=	ENSP00000484108.1:n.*419G=
ENST00000621629.4:c.*419G=	ENSP00000478747.1:n.*419G=
ENST00000621817.1:c.*708G=	ENSP00000481634.1:n.*708G=
NM_001130997.2:c.543G=	NP_001124469.1:p.Ala181=
NM_152274.4:c.543G=	NP_689487.2:p.Ala181=
XM_005277920.3:c.513G=	XP_005277977.1:p.Ala171=
XM_005277921.3:c.513G=	XP_005277978.1:p.Ala171=
XM_011531213.1:c.417G=	XP_011529515.1:p.Ala139=
XM_011531214.1:c.417G=	XP_011529516.1:p.Ala139=
XM_011531215.1:c.417G=	XP_011529517.1:p.Ala139=
XM_005277920.4:c.513G=	XP_005277977.1:p.Ala171=
XM_005277921.4:c.513G=	XP_005277978.1:p.Ala171=
XM_011531214.2:c.417G=	XP_011529516.1:p.Ala139=
XM_011531215.2:c.417G=	XP_011529517.1:p.Ala139=
XR_002958810.1:n.2448G=
NM_152274.5:c.543G= MANE Select	NP_689487.2:p.Ala181=
NM_001130997.3:c.543G=	NP_001124469.1:p.Ala181=