Canonical Allele Identifier: CA2466399723

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592531_153592535delinsACCTC , CM000685.2:g.153592531_153592535delinsACCTC	GRCh38
NC_000023.10:g.152857989_152857993delinsACCTC , CM000685.1:g.152857989_152857993delinsACCTC	GRCh37
NC_000023.9:g.152511183_152511187delinsACCTC	NCBI36
NG_008393.2:g.11643_11647delinsGAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.628_632delinsGAGGT MANE Select	ENSP00000461135.1:p.Glu210=
ENST00000429336.5:c.193+2012_193+2016delinsGAGGT
ENST00000440428.5:c.628_632delinsGAGGT	ENSP00000402949.2:p.Glu210=
ENST00000576892.7:c.628_632delinsGAGGT	ENSP00000461135.1:p.Glu210=
ENST00000614850.1:c.277+3469_277+3473delinsGAGGT
ENST00000614851.4:c.449_453delinsGAGGT
ENST00000620088.4:c.*504_*508delinsGAGGT	ENSP00000484108.1:n.*504_*508delinsGAGGT
ENST00000621629.4:c.*504_*508delinsGAGGT	ENSP00000478747.1:n.*504_*508delinsGAGGT
NM_001130997.2:c.628_632delinsGAGGT	NP_001124469.1:p.Glu210=
NM_152274.4:c.628_632delinsGAGGT	NP_689487.2:p.Glu210=
XM_005277920.3:c.598_602delinsGAGGT	XP_005277977.1:p.Glu200=
XM_005277921.3:c.598_602delinsGAGGT	XP_005277978.1:p.Glu200=
XM_011531213.1:c.502_506delinsGAGGT	XP_011529515.1:p.Glu168=
XM_011531214.1:c.502_506delinsGAGGT	XP_011529516.1:p.Glu168=
XM_011531215.1:c.502_506delinsGAGGT	XP_011529517.1:p.Glu168=
XM_005277920.4:c.598_602delinsGAGGT	XP_005277977.1:p.Glu200=
XM_005277921.4:c.598_602delinsGAGGT	XP_005277978.1:p.Glu200=
XM_011531214.2:c.502_506delinsGAGGT	XP_011529516.1:p.Glu168=
XM_011531215.2:c.502_506delinsGAGGT	XP_011529517.1:p.Glu168=
XR_002958810.1:n.2533_2537delinsGAGGT
NM_152274.5:c.628_632delinsGAGGT MANE Select	NP_689487.2:p.Glu210=
NM_001130997.3:c.628_632delinsGAGGT	NP_001124469.1:p.Glu210=