Canonical Allele Identifier: CA2466399734

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592558A= , CM000685.2:g.153592558A=	GRCh38
NC_000023.10:g.152858016A= , CM000685.1:g.152858016A=	GRCh37
NC_000023.9:g.152511210A=	NCBI36
NG_008393.2:g.11620T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.605T= MANE Select	ENSP00000461135.1:p.Val202=
ENST00000429336.5:c.193+1989T=
ENST00000440428.5:c.605T=	ENSP00000402949.2:p.Val202=
ENST00000576892.7:c.605T=	ENSP00000461135.1:p.Val202=
ENST00000614850.1:c.277+3446T=
ENST00000614851.4:c.426T=
ENST00000620088.4:c.*481T=	ENSP00000484108.1:n.*481T=
ENST00000621629.4:c.*481T=	ENSP00000478747.1:n.*481T=
NM_001130997.2:c.605T=	NP_001124469.1:p.Val202=
NM_152274.4:c.605T=	NP_689487.2:p.Val202=
XM_005277920.3:c.575T=	XP_005277977.1:p.Val192=
XM_005277921.3:c.575T=	XP_005277978.1:p.Val192=
XM_011531213.1:c.479T=	XP_011529515.1:p.Val160=
XM_011531214.1:c.479T=	XP_011529516.1:p.Val160=
XM_011531215.1:c.479T=	XP_011529517.1:p.Val160=
XM_005277920.4:c.575T=	XP_005277977.1:p.Val192=
XM_005277921.4:c.575T=	XP_005277978.1:p.Val192=
XM_011531214.2:c.479T=	XP_011529516.1:p.Val160=
XM_011531215.2:c.479T=	XP_011529517.1:p.Val160=
XR_002958810.1:n.2510T=
NM_152274.5:c.605T= MANE Select	NP_689487.2:p.Val202=
NM_001130997.3:c.605T=	NP_001124469.1:p.Val202=