Canonical Allele Identifier: CA415087941

Gene: CCNQ

Linked Data

• MyVariant Identifiers: chrX:g.152858084A>C (hg19) ; chrX:g.153592626A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592626A>C , CM000685.2:g.153592626A>C	GRCh38
NC_000023.10:g.152858084A>C , CM000685.1:g.152858084A>C	GRCh37
NC_000023.9:g.152511278A>C	NCBI36
NG_008393.2:g.11552T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.537T>G MANE Select	ENSP00000461135.1:p.His179Gln
ENST00000429336.5:c.193+1921T>G
ENST00000440428.5:c.537T>G	ENSP00000402949.2:p.His179Gln
ENST00000482182.3:c.411T>G	ENSP00000466345.1:p.His137Gln
ENST00000576892.7:c.537T>G	ENSP00000461135.1:p.His179Gln
ENST00000614850.1:c.277+3378T>G
ENST00000614851.4:c.358T>G
ENST00000620088.4:c.*413T>G	ENSP00000484108.1:n.*413T>G
ENST00000621629.4:c.*413T>G	ENSP00000478747.1:n.*413T>G
ENST00000621817.1:c.*702T>G	ENSP00000481634.1:n.*702T>G
NM_001130997.2:c.537T>G	NP_001124469.1:p.His179Gln
NM_152274.4:c.537T>G	NP_689487.2:p.His179Gln
XM_005277920.3:c.507T>G	XP_005277977.1:p.His169Gln
XM_005277921.3:c.507T>G	XP_005277978.1:p.His169Gln
XM_011531213.1:c.411T>G	XP_011529515.1:p.His137Gln
XM_011531214.1:c.411T>G	XP_011529516.1:p.His137Gln
XM_011531215.1:c.411T>G	XP_011529517.1:p.His137Gln
XM_005277920.4:c.507T>G	XP_005277977.1:p.His169Gln
XM_005277921.4:c.507T>G	XP_005277978.1:p.His169Gln
XM_011531214.2:c.411T>G	XP_011529516.1:p.His137Gln
XM_011531215.2:c.411T>G	XP_011529517.1:p.His137Gln
XR_002958810.1:n.2442T>G
NM_152274.5:c.537T>G MANE Select	NP_689487.2:p.His179Gln
NM_001130997.3:c.537T>G	NP_001124469.1:p.His179Gln