Canonical Allele Identifier: CA2466399682
Gene: CCNQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153592386A= , CM000685.2:g.153592386A= GRCh38
NC_000023.10:g.152857844A= , CM000685.1:g.152857844A= GRCh37
NC_000023.9:g.152511038A= NCBI36
NG_008393.2:g.11792T=

Transcript Alleles

HGVS Amino-acid change
ENST00000576892.8:c.657+120T= MANE Select ENSP00000461135.1:n.657+120T=
ENST00000429336.5:c.193+2161T=
ENST00000440428.5:c.657+120T= ENSP00000402949.2:n.657+120T=
ENST00000576892.7:c.657+120T= ENSP00000461135.1:n.657+120T=
ENST00000614850.1:c.277+3618T=
ENST00000614851.4:c.478+120T=
ENST00000620088.4:c.*533+120T= ENSP00000484108.1:n.*533+120T=
ENST00000621629.4:c.*533+120T= ENSP00000478747.1:n.*533+120T=
NM_001130997.2:c.657+120T= NP_001124469.1:n.657+120T=
NM_152274.4:c.657+120T= NP_689487.2:n.657+120T=
XM_005277920.3:c.627+120T= XP_005277977.1:n.627+120T=
XM_005277921.3:c.627+120T= XP_005277978.1:n.627+120T=
XM_011531213.1:c.531+120T= XP_011529515.1:n.531+120T=
XM_011531214.1:c.531+120T= XP_011529516.1:n.531+120T=
XM_011531215.1:c.531+120T= XP_011529517.1:n.531+120T=
XM_005277920.4:c.627+120T= XP_005277977.1:n.627+120T=
XM_005277921.4:c.627+120T= XP_005277978.1:n.627+120T=
XM_011531214.2:c.531+120T= XP_011529516.1:n.531+120T=
XM_011531215.2:c.531+120T= XP_011529517.1:n.531+120T=
XR_002958810.1:n.2562+120T=
NM_152274.5:c.657+120T= MANE Select NP_689487.2:n.657+120T=
NM_001130997.3:c.657+120T= NP_001124469.1:n.657+120T=