Canonical Allele Identifier: CA415087321

Gene: CCNQ

Linked Data

• COSMIC: COSM5697370
• MyVariant Identifiers: chrX:g.152857987C>A (hg19) ; chrX:g.153592529C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592529C>A , CM000685.2:g.153592529C>A	GRCh38
NC_000023.10:g.152857987C>A , CM000685.1:g.152857987C>A	GRCh37
NC_000023.9:g.152511181C>A	NCBI36
NG_008393.2:g.11649G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.634G>T MANE Select	ENSP00000461135.1:p.Glu212Ter
ENST00000429336.5:c.193+2018G>T
ENST00000440428.5:c.634G>T	ENSP00000402949.2:p.Glu212Ter
ENST00000576892.7:c.634G>T	ENSP00000461135.1:p.Glu212Ter
ENST00000614850.1:c.277+3475G>T
ENST00000614851.4:c.455G>T
ENST00000620088.4:c.*510G>T	ENSP00000484108.1:n.*510G>T
ENST00000621629.4:c.*510G>T	ENSP00000478747.1:n.*510G>T
NM_001130997.2:c.634G>T	NP_001124469.1:p.Glu212Ter
NM_152274.4:c.634G>T	NP_689487.2:p.Glu212Ter
XM_005277920.3:c.604G>T	XP_005277977.1:p.Glu202Ter
XM_005277921.3:c.604G>T	XP_005277978.1:p.Glu202Ter
XM_011531213.1:c.508G>T	XP_011529515.1:p.Glu170Ter
XM_011531214.1:c.508G>T	XP_011529516.1:p.Glu170Ter
XM_011531215.1:c.508G>T	XP_011529517.1:p.Glu170Ter
XM_005277920.4:c.604G>T	XP_005277977.1:p.Glu202Ter
XM_005277921.4:c.604G>T	XP_005277978.1:p.Glu202Ter
XM_011531214.2:c.508G>T	XP_011529516.1:p.Glu170Ter
XM_011531215.2:c.508G>T	XP_011529517.1:p.Glu170Ter
XR_002958810.1:n.2539G>T
NM_152274.5:c.634G>T MANE Select	NP_689487.2:p.Glu212Ter
NM_001130997.3:c.634G>T	NP_001124469.1:p.Glu212Ter