Canonical Allele Identifier: CA519214575

Gene: CCNQ

Linked Data

• MyVariant Identifiers: chrX:g.152858162C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592704C>T , CM000685.2:g.153592704C>T	GRCh38
NC_000023.10:g.152858162C>T , CM000685.1:g.152858162C>T	GRCh37
NC_000023.9:g.152511356C>T	NCBI36
NG_008393.2:g.11474G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.459G>A MANE Select	ENSP00000461135.1:p.Gln153=
ENST00000429336.5:c.193+1843G>A
ENST00000440428.5:c.459G>A	ENSP00000402949.2:p.Gln153=
ENST00000482182.3:c.333G>A	ENSP00000466345.1:p.Gln111=
ENST00000576892.7:c.459G>A	ENSP00000461135.1:p.Gln153=
ENST00000614850.1:c.277+3300G>A
ENST00000614851.4:c.280G>A
ENST00000620088.4:c.*335G>A	ENSP00000484108.1:n.*335G>A
ENST00000621629.4:c.*335G>A	ENSP00000478747.1:n.*335G>A
ENST00000621817.1:c.*624G>A	ENSP00000481634.1:n.*624G>A
NM_001130997.2:c.459G>A	NP_001124469.1:p.Gln153=
NM_152274.4:c.459G>A	NP_689487.2:p.Gln153=
XM_005277920.3:c.430-1G>A	XP_005277977.1:n.430-1G>A
XM_005277921.3:c.430-1G>A	XP_005277978.1:n.430-1G>A
XM_011531213.1:c.333G>A	XP_011529515.1:p.Gln111=
XM_011531214.1:c.333G>A	XP_011529516.1:p.Gln111=
XM_011531215.1:c.333G>A	XP_011529517.1:p.Gln111=
XM_005277920.4:c.430-1G>A	XP_005277977.1:n.430-1G>A
XM_005277921.4:c.430-1G>A	XP_005277978.1:n.430-1G>A
XM_011531214.2:c.333G>A	XP_011529516.1:p.Gln111=
XM_011531215.2:c.333G>A	XP_011529517.1:p.Gln111=
XR_002958810.1:n.2364G>A
NM_152274.5:c.459G>A MANE Select	NP_689487.2:p.Gln153=
NM_001130997.3:c.459G>A	NP_001124469.1:p.Gln153=