Canonical Allele Identifier: CA519213721

Gene: CCNQ

Linked Data

• MyVariant Identifiers: chrX:g.152858039C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592581C>G , CM000685.2:g.153592581C>G	GRCh38
NC_000023.10:g.152858039C>G , CM000685.1:g.152858039C>G	GRCh37
NC_000023.9:g.152511233C>G	NCBI36
NG_008393.2:g.11597G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.582G>C MANE Select	ENSP00000461135.1:p.Ala194=
ENST00000429336.5:c.193+1966G>C
ENST00000440428.5:c.582G>C	ENSP00000402949.2:p.Ala194=
ENST00000576892.7:c.582G>C	ENSP00000461135.1:p.Ala194=
ENST00000614850.1:c.277+3423G>C
ENST00000614851.4:c.403G>C
ENST00000620088.4:c.*458G>C	ENSP00000484108.1:n.*458G>C
ENST00000621629.4:c.*458G>C	ENSP00000478747.1:n.*458G>C
ENST00000621817.1:c.*747G>C	ENSP00000481634.1:n.*747G>C
NM_001130997.2:c.582G>C	NP_001124469.1:p.Ala194=
NM_152274.4:c.582G>C	NP_689487.2:p.Ala194=
XM_005277920.3:c.552G>C	XP_005277977.1:p.Ala184=
XM_005277921.3:c.552G>C	XP_005277978.1:p.Ala184=
XM_011531213.1:c.456G>C	XP_011529515.1:p.Ala152=
XM_011531214.1:c.456G>C	XP_011529516.1:p.Ala152=
XM_011531215.1:c.456G>C	XP_011529517.1:p.Ala152=
XM_005277920.4:c.552G>C	XP_005277977.1:p.Ala184=
XM_005277921.4:c.552G>C	XP_005277978.1:p.Ala184=
XM_011531214.2:c.456G>C	XP_011529516.1:p.Ala152=
XM_011531215.2:c.456G>C	XP_011529517.1:p.Ala152=
XR_002958810.1:n.2487G>C
NM_152274.5:c.582G>C MANE Select	NP_689487.2:p.Ala194=
NM_001130997.3:c.582G>C	NP_001124469.1:p.Ala194=