Canonical Allele Identifier: CA2695026087

Gene: CCNQ

Linked Data

• gnomAD v4: X-153592456-ACTTCCAGAGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592457_153592467del , CM000685.2:g.153592457_153592467del	GRCh38
NC_000023.10:g.152857915_152857925del , CM000685.1:g.152857915_152857925del	GRCh37
NC_000023.9:g.152511109_152511119del	NCBI36
NG_008393.2:g.11711_11721del

Transcript Alleles

HGVS	Amino-acid change
ENST00000576892.8:c.657+39_657+49del MANE Select	ENSP00000461135.1:n.657+39_657+49del
ENST00000429336.5:c.193+2080_193+2090del
ENST00000440428.5:c.657+39_657+49del	ENSP00000402949.2:n.657+39_657+49del
ENST00000576892.7:c.657+39_657+49del	ENSP00000461135.1:n.657+39_657+49del
ENST00000614850.1:c.277+3537_277+3547del
ENST00000614851.4:c.478+39_478+49del
ENST00000620088.4:c.*533+39_*533+49del	ENSP00000484108.1:n.*533+39_*533+49del
ENST00000621629.4:c.*533+39_*533+49del	ENSP00000478747.1:n.*533+39_*533+49del
NM_001130997.2:c.657+39_657+49del	NP_001124469.1:n.657+39_657+49del
NM_152274.4:c.657+39_657+49del	NP_689487.2:n.657+39_657+49del
XM_005277920.3:c.627+39_627+49del	XP_005277977.1:n.627+39_627+49del
XM_005277921.3:c.627+39_627+49del	XP_005277978.1:n.627+39_627+49del
XM_011531213.1:c.531+39_531+49del	XP_011529515.1:n.531+39_531+49del
XM_011531214.1:c.531+39_531+49del	XP_011529516.1:n.531+39_531+49del
XM_011531215.1:c.531+39_531+49del	XP_011529517.1:n.531+39_531+49del
XM_005277920.4:c.627+39_627+49del	XP_005277977.1:n.627+39_627+49del
XM_005277921.4:c.627+39_627+49del	XP_005277978.1:n.627+39_627+49del
XM_011531214.2:c.531+39_531+49del	XP_011529516.1:n.531+39_531+49del
XM_011531215.2:c.531+39_531+49del	XP_011529517.1:n.531+39_531+49del
XR_002958810.1:n.2562+39_2562+49del
NM_152274.5:c.657+39_657+49del MANE Select	NP_689487.2:n.657+39_657+49del
NM_001130997.3:c.657+39_657+49del	NP_001124469.1:n.657+39_657+49del