Canonical Allele Identifier: CA415087328

Gene: CCNQ

Linked Data

• MyVariant Identifiers: chrX:g.152857989A>C (hg19) ; chrX:g.153592531A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592531A>C , CM000685.2:g.153592531A>C	GRCh38
NC_000023.10:g.152857989A>C , CM000685.1:g.152857989A>C	GRCh37
NC_000023.9:g.152511183A>C	NCBI36
NG_008393.2:g.11647T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.632T>G MANE Select	ENSP00000461135.1:p.Val211Gly
ENST00000429336.5:c.193+2016T>G
ENST00000440428.5:c.632T>G	ENSP00000402949.2:p.Val211Gly
ENST00000576892.7:c.632T>G	ENSP00000461135.1:p.Val211Gly
ENST00000614850.1:c.277+3473T>G
ENST00000614851.4:c.453T>G
ENST00000620088.4:c.*508T>G	ENSP00000484108.1:n.*508T>G
ENST00000621629.4:c.*508T>G	ENSP00000478747.1:n.*508T>G
NM_001130997.2:c.632T>G	NP_001124469.1:p.Val211Gly
NM_152274.4:c.632T>G	NP_689487.2:p.Val211Gly
XM_005277920.3:c.602T>G	XP_005277977.1:p.Val201Gly
XM_005277921.3:c.602T>G	XP_005277978.1:p.Val201Gly
XM_011531213.1:c.506T>G	XP_011529515.1:p.Val169Gly
XM_011531214.1:c.506T>G	XP_011529516.1:p.Val169Gly
XM_011531215.1:c.506T>G	XP_011529517.1:p.Val169Gly
XM_005277920.4:c.602T>G	XP_005277977.1:p.Val201Gly
XM_005277921.4:c.602T>G	XP_005277978.1:p.Val201Gly
XM_011531214.2:c.506T>G	XP_011529516.1:p.Val169Gly
XM_011531215.2:c.506T>G	XP_011529517.1:p.Val169Gly
XR_002958810.1:n.2537T>G
NM_152274.5:c.632T>G MANE Select	NP_689487.2:p.Val211Gly
NM_001130997.3:c.632T>G	NP_001124469.1:p.Val211Gly