Canonical Allele Identifier: CA2466399747

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592590G= , CM000685.2:g.153592590G=	GRCh38
NC_000023.10:g.152858048G= , CM000685.1:g.152858048G=	GRCh37
NC_000023.9:g.152511242G=	NCBI36
NG_008393.2:g.11588C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.573C= MANE Select	ENSP00000461135.1:p.Ile191=
ENST00000429336.5:c.193+1957C=
ENST00000440428.5:c.573C=	ENSP00000402949.2:p.Ile191=
ENST00000576892.7:c.573C=	ENSP00000461135.1:p.Ile191=
ENST00000614850.1:c.277+3414C=
ENST00000614851.4:c.394C=
ENST00000620088.4:c.*449C=	ENSP00000484108.1:n.*449C=
ENST00000621629.4:c.*449C=	ENSP00000478747.1:n.*449C=
ENST00000621817.1:c.*738C=	ENSP00000481634.1:n.*738C=
NM_001130997.2:c.573C=	NP_001124469.1:p.Ile191=
NM_152274.4:c.573C=	NP_689487.2:p.Ile191=
XM_005277920.3:c.543C=	XP_005277977.1:p.Ile181=
XM_005277921.3:c.543C=	XP_005277978.1:p.Ile181=
XM_011531213.1:c.447C=	XP_011529515.1:p.Ile149=
XM_011531214.1:c.447C=	XP_011529516.1:p.Ile149=
XM_011531215.1:c.447C=	XP_011529517.1:p.Ile149=
XM_005277920.4:c.543C=	XP_005277977.1:p.Ile181=
XM_005277921.4:c.543C=	XP_005277978.1:p.Ile181=
XM_011531214.2:c.447C=	XP_011529516.1:p.Ile149=
XM_011531215.2:c.447C=	XP_011529517.1:p.Ile149=
XR_002958810.1:n.2478C=
NM_152274.5:c.573C= MANE Select	NP_689487.2:p.Ile191=
NM_001130997.3:c.573C=	NP_001124469.1:p.Ile191=