Canonical Allele Identifier: CA415087586

Gene: CCNQ

Linked Data

• MyVariant Identifiers: chrX:g.152858032A>G (hg19) ; chrX:g.153592574A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592574A>G , CM000685.2:g.153592574A>G	GRCh38
NC_000023.10:g.152858032A>G , CM000685.1:g.152858032A>G	GRCh37
NC_000023.9:g.152511226A>G	NCBI36
NG_008393.2:g.11604T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.589T>C MANE Select	ENSP00000461135.1:p.Tyr197His
ENST00000429336.5:c.193+1973T>C
ENST00000440428.5:c.589T>C	ENSP00000402949.2:p.Tyr197His
ENST00000576892.7:c.589T>C	ENSP00000461135.1:p.Tyr197His
ENST00000614850.1:c.277+3430T>C
ENST00000614851.4:c.410T>C
ENST00000620088.4:c.*465T>C	ENSP00000484108.1:n.*465T>C
ENST00000621629.4:c.*465T>C	ENSP00000478747.1:n.*465T>C
NM_001130997.2:c.589T>C	NP_001124469.1:p.Tyr197His
NM_152274.4:c.589T>C	NP_689487.2:p.Tyr197His
XM_005277920.3:c.559T>C	XP_005277977.1:p.Tyr187His
XM_005277921.3:c.559T>C	XP_005277978.1:p.Tyr187His
XM_011531213.1:c.463T>C	XP_011529515.1:p.Tyr155His
XM_011531214.1:c.463T>C	XP_011529516.1:p.Tyr155His
XM_011531215.1:c.463T>C	XP_011529517.1:p.Tyr155His
XM_005277920.4:c.559T>C	XP_005277977.1:p.Tyr187His
XM_005277921.4:c.559T>C	XP_005277978.1:p.Tyr187His
XM_011531214.2:c.463T>C	XP_011529516.1:p.Tyr155His
XM_011531215.2:c.463T>C	XP_011529517.1:p.Tyr155His
XR_002958810.1:n.2494T>C
NM_152274.5:c.589T>C MANE Select	NP_689487.2:p.Tyr197His
NM_001130997.3:c.589T>C	NP_001124469.1:p.Tyr197His