Canonical Allele Identifier: CA2839966596

Gene: CCNQ

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592672dup , CM000685.2:g.153592672dup	GRCh38
NC_000023.10:g.152858130dup , CM000685.1:g.152858130dup	GRCh37
NC_000023.9:g.152511324dup	NCBI36
NG_008393.2:g.11509dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.494dup MANE Select	ENSP00000461135.1:p.Val166CysfsTer?
ENST00000429336.5:c.193+1878dup
ENST00000440428.5:c.494dup	ENSP00000402949.2:p.Val166CysfsTer?
ENST00000482182.3:c.368dup	ENSP00000466345.1:p.Val124CysfsTer?
ENST00000576892.7:c.494dup	ENSP00000461135.1:p.Val166CysfsTer?
ENST00000614850.1:c.277+3335dup
ENST00000614851.4:c.315dup
ENST00000620088.4:c.*370dup	ENSP00000484108.1:n.*370dup
ENST00000621629.4:c.*370dup	ENSP00000478747.1:n.*370dup
ENST00000621817.1:c.*659dup	ENSP00000481634.1:n.*659dup
NM_001130997.2:c.494dup	NP_001124469.1:p.Val166CysfsTer?
NM_152274.4:c.494dup	NP_689487.2:p.Val166CysfsTer?
XM_005277920.3:c.464dup	XP_005277977.1:p.Val156CysfsTer?
XM_005277921.3:c.464dup	XP_005277978.1:p.Val156CysfsTer?
XM_011531213.1:c.368dup	XP_011529515.1:p.Val124CysfsTer?
XM_011531214.1:c.368dup	XP_011529516.1:p.Val124CysfsTer?
XM_011531215.1:c.368dup	XP_011529517.1:p.Val124CysfsTer?
XM_005277920.4:c.464dup	XP_005277977.1:p.Val156CysfsTer?
XM_005277921.4:c.464dup	XP_005277978.1:p.Val156CysfsTer?
XM_011531214.2:c.368dup	XP_011529516.1:p.Val124CysfsTer?
XM_011531215.2:c.368dup	XP_011529517.1:p.Val124CysfsTer?
XR_002958810.1:n.2399dup
NM_152274.5:c.494dup MANE Select	NP_689487.2:p.Val166CysfsTer?
NM_001130997.3:c.494dup	NP_001124469.1:p.Val166CysfsTer?