Canonical Allele Identifier: CA2579728647

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592466G>T , CM000685.2:g.153592466G>T	GRCh38
NC_000023.10:g.152857924G>T , CM000685.1:g.152857924G>T	GRCh37
NC_000023.9:g.152511118G>T	NCBI36
NG_008393.2:g.11712C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000576892.8:c.657+40C>A MANE Select	ENSP00000461135.1:n.657+40C>A
ENST00000429336.5:c.193+2081C>A
ENST00000440428.5:c.657+40C>A	ENSP00000402949.2:n.657+40C>A
ENST00000576892.7:c.657+40C>A	ENSP00000461135.1:n.657+40C>A
ENST00000614850.1:c.277+3538C>A
ENST00000614851.4:c.478+40C>A
ENST00000620088.4:c.*533+40C>A	ENSP00000484108.1:n.*533+40C>A
ENST00000621629.4:c.*533+40C>A	ENSP00000478747.1:n.*533+40C>A
NM_001130997.2:c.657+40C>A	NP_001124469.1:n.657+40C>A
NM_152274.4:c.657+40C>A	NP_689487.2:n.657+40C>A
XM_005277920.3:c.627+40C>A	XP_005277977.1:n.627+40C>A
XM_005277921.3:c.627+40C>A	XP_005277978.1:n.627+40C>A
XM_011531213.1:c.531+40C>A	XP_011529515.1:n.531+40C>A
XM_011531214.1:c.531+40C>A	XP_011529516.1:n.531+40C>A
XM_011531215.1:c.531+40C>A	XP_011529517.1:n.531+40C>A
XM_005277920.4:c.627+40C>A	XP_005277977.1:n.627+40C>A
XM_005277921.4:c.627+40C>A	XP_005277978.1:n.627+40C>A
XM_011531214.2:c.531+40C>A	XP_011529516.1:n.531+40C>A
XM_011531215.2:c.531+40C>A	XP_011529517.1:n.531+40C>A
XR_002958810.1:n.2562+40C>A
NM_152274.5:c.657+40C>A MANE Select	NP_689487.2:n.657+40C>A
NM_001130997.3:c.657+40C>A	NP_001124469.1:n.657+40C>A