Canonical Allele Identifier: CA519213861

Gene: CCNQ

Linked Data

• MyVariant Identifiers: chrX:g.152858060C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592602C>T , CM000685.2:g.153592602C>T	GRCh38
NC_000023.10:g.152858060C>T , CM000685.1:g.152858060C>T	GRCh37
NC_000023.9:g.152511254C>T	NCBI36
NG_008393.2:g.11576G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.561G>A MANE Select	ENSP00000461135.1:p.Gln187=
ENST00000429336.5:c.193+1945G>A
ENST00000440428.5:c.561G>A	ENSP00000402949.2:p.Gln187=
ENST00000576892.7:c.561G>A	ENSP00000461135.1:p.Gln187=
ENST00000614850.1:c.277+3402G>A
ENST00000614851.4:c.382G>A
ENST00000620088.4:c.*437G>A	ENSP00000484108.1:n.*437G>A
ENST00000621629.4:c.*437G>A	ENSP00000478747.1:n.*437G>A
ENST00000621817.1:c.*726G>A	ENSP00000481634.1:n.*726G>A
NM_001130997.2:c.561G>A	NP_001124469.1:p.Gln187=
NM_152274.4:c.561G>A	NP_689487.2:p.Gln187=
XM_005277920.3:c.531G>A	XP_005277977.1:p.Gln177=
XM_005277921.3:c.531G>A	XP_005277978.1:p.Gln177=
XM_011531213.1:c.435G>A	XP_011529515.1:p.Gln145=
XM_011531214.1:c.435G>A	XP_011529516.1:p.Gln145=
XM_011531215.1:c.435G>A	XP_011529517.1:p.Gln145=
XM_005277920.4:c.531G>A	XP_005277977.1:p.Gln177=
XM_005277921.4:c.531G>A	XP_005277978.1:p.Gln177=
XM_011531214.2:c.435G>A	XP_011529516.1:p.Gln145=
XM_011531215.2:c.435G>A	XP_011529517.1:p.Gln145=
XR_002958810.1:n.2466G>A
NM_152274.5:c.561G>A MANE Select	NP_689487.2:p.Gln187=
NM_001130997.3:c.561G>A	NP_001124469.1:p.Gln187=