Canonical Allele Identifier: CA2695026111

Gene: CCNQ

Linked Data

• gnomAD v4: X-153592757-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592757T>C , CM000685.2:g.153592757T>C	GRCh38
NC_000023.10:g.152858215T>C , CM000685.1:g.152858215T>C	GRCh37
NC_000023.9:g.152511409T>C	NCBI36
NG_008393.2:g.11421A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.430-24A>G MANE Select	ENSP00000461135.1:n.430-24A>G
ENST00000429336.5:c.193+1790A>G
ENST00000440428.5:c.430-24A>G	ENSP00000402949.2:n.430-24A>G
ENST00000482182.3:c.304-24A>G	ENSP00000466345.1:n.304-24A>G
ENST00000576892.7:c.430-24A>G	ENSP00000461135.1:n.430-24A>G
ENST00000614850.1:c.277+3247A>G
ENST00000614851.4:c.251-24A>G
ENST00000620088.4:c.*306-24A>G	ENSP00000484108.1:n.*306-24A>G
ENST00000621629.4:c.*306-24A>G	ENSP00000478747.1:n.*306-24A>G
ENST00000621817.1:c.*595-24A>G	ENSP00000481634.1:n.*595-24A>G
NM_001130997.2:c.430-24A>G	NP_001124469.1:n.430-24A>G
NM_152274.4:c.430-24A>G	NP_689487.2:n.430-24A>G
XM_005277920.3:c.430-54A>G	XP_005277977.1:n.430-54A>G
XM_005277921.3:c.430-54A>G	XP_005277978.1:n.430-54A>G
XM_011531213.1:c.304-24A>G	XP_011529515.1:n.304-24A>G
XM_011531214.1:c.304-24A>G	XP_011529516.1:n.304-24A>G
XM_011531215.1:c.304-24A>G	XP_011529517.1:n.304-24A>G
XM_005277920.4:c.430-54A>G	XP_005277977.1:n.430-54A>G
XM_005277921.4:c.430-54A>G	XP_005277978.1:n.430-54A>G
XM_011531214.2:c.304-24A>G	XP_011529516.1:n.304-24A>G
XM_011531215.2:c.304-24A>G	XP_011529517.1:n.304-24A>G
XR_002958810.1:n.2311A>G
NM_152274.5:c.430-24A>G MANE Select	NP_689487.2:n.430-24A>G
NM_001130997.3:c.430-24A>G	NP_001124469.1:n.430-24A>G