Canonical Allele Identifier: CA415088070

Gene: CCNQ

Linked Data

• MyVariant Identifiers: chrX:g.152858108C>T (hg19) ; chrX:g.153592650C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592650C>T , CM000685.2:g.153592650C>T	GRCh38
NC_000023.10:g.152858108C>T , CM000685.1:g.152858108C>T	GRCh37
NC_000023.9:g.152511302C>T	NCBI36
NG_008393.2:g.11528G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.513G>A MANE Select	ENSP00000461135.1:p.Trp171Ter
ENST00000429336.5:c.193+1897G>A
ENST00000440428.5:c.513G>A	ENSP00000402949.2:p.Trp171Ter
ENST00000482182.3:c.387G>A	ENSP00000466345.1:p.Trp129Ter
ENST00000576892.7:c.513G>A	ENSP00000461135.1:p.Trp171Ter
ENST00000614850.1:c.277+3354G>A
ENST00000614851.4:c.334G>A
ENST00000620088.4:c.*389G>A	ENSP00000484108.1:n.*389G>A
ENST00000621629.4:c.*389G>A	ENSP00000478747.1:n.*389G>A
ENST00000621817.1:c.*678G>A	ENSP00000481634.1:n.*678G>A
NM_001130997.2:c.513G>A	NP_001124469.1:p.Trp171Ter
NM_152274.4:c.513G>A	NP_689487.2:p.Trp171Ter
XM_005277920.3:c.483G>A	XP_005277977.1:p.Trp161Ter
XM_005277921.3:c.483G>A	XP_005277978.1:p.Trp161Ter
XM_011531213.1:c.387G>A	XP_011529515.1:p.Trp129Ter
XM_011531214.1:c.387G>A	XP_011529516.1:p.Trp129Ter
XM_011531215.1:c.387G>A	XP_011529517.1:p.Trp129Ter
XM_005277920.4:c.483G>A	XP_005277977.1:p.Trp161Ter
XM_005277921.4:c.483G>A	XP_005277978.1:p.Trp161Ter
XM_011531214.2:c.387G>A	XP_011529516.1:p.Trp129Ter
XM_011531215.2:c.387G>A	XP_011529517.1:p.Trp129Ter
XR_002958810.1:n.2418G>A
NM_152274.5:c.513G>A MANE Select	NP_689487.2:p.Trp171Ter
NM_001130997.3:c.513G>A	NP_001124469.1:p.Trp171Ter