Canonical Allele Identifier: CA519214077

Gene: CCNQ

Linked Data

• MyVariant Identifiers: chrX:g.152858090G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592632G>A , CM000685.2:g.153592632G>A	GRCh38
NC_000023.10:g.152858090G>A , CM000685.1:g.152858090G>A	GRCh37
NC_000023.9:g.152511284G>A	NCBI36
NG_008393.2:g.11546C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.531C>T MANE Select	ENSP00000461135.1:p.Ser177=
ENST00000429336.5:c.193+1915C>T
ENST00000440428.5:c.531C>T	ENSP00000402949.2:p.Ser177=
ENST00000482182.3:c.405C>T	ENSP00000466345.1:p.Ser135=
ENST00000576892.7:c.531C>T	ENSP00000461135.1:p.Ser177=
ENST00000614850.1:c.277+3372C>T
ENST00000614851.4:c.352C>T
ENST00000620088.4:c.*407C>T	ENSP00000484108.1:n.*407C>T
ENST00000621629.4:c.*407C>T	ENSP00000478747.1:n.*407C>T
ENST00000621817.1:c.*696C>T	ENSP00000481634.1:n.*696C>T
NM_001130997.2:c.531C>T	NP_001124469.1:p.Ser177=
NM_152274.4:c.531C>T	NP_689487.2:p.Ser177=
XM_005277920.3:c.501C>T	XP_005277977.1:p.Ser167=
XM_005277921.3:c.501C>T	XP_005277978.1:p.Ser167=
XM_011531213.1:c.405C>T	XP_011529515.1:p.Ser135=
XM_011531214.1:c.405C>T	XP_011529516.1:p.Ser135=
XM_011531215.1:c.405C>T	XP_011529517.1:p.Ser135=
XM_005277920.4:c.501C>T	XP_005277977.1:p.Ser167=
XM_005277921.4:c.501C>T	XP_005277978.1:p.Ser167=
XM_011531214.2:c.405C>T	XP_011529516.1:p.Ser135=
XM_011531215.2:c.405C>T	XP_011529517.1:p.Ser135=
XR_002958810.1:n.2436C>T
NM_152274.5:c.531C>T MANE Select	NP_689487.2:p.Ser177=
NM_001130997.3:c.531C>T	NP_001124469.1:p.Ser177=