Canonical Allele Identifier: CA415088404

Gene: CCNQ

Linked Data

• MyVariant Identifiers: chrX:g.152858161T>G (hg19) ; chrX:g.153592703T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153592703T>G , CM000685.2:g.153592703T>G	GRCh38
NC_000023.10:g.152858161T>G , CM000685.1:g.152858161T>G	GRCh37
NC_000023.9:g.152511355T>G	NCBI36
NG_008393.2:g.11475A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576892.8:c.460A>C MANE Select	ENSP00000461135.1:p.Asn154His
ENST00000429336.5:c.193+1844A>C
ENST00000440428.5:c.460A>C	ENSP00000402949.2:p.Asn154His
ENST00000482182.3:c.334A>C	ENSP00000466345.1:p.Asn112His
ENST00000576892.7:c.460A>C	ENSP00000461135.1:p.Asn154His
ENST00000614850.1:c.277+3301A>C
ENST00000614851.4:c.281A>C
ENST00000620088.4:c.*336A>C	ENSP00000484108.1:n.*336A>C
ENST00000621629.4:c.*336A>C	ENSP00000478747.1:n.*336A>C
ENST00000621817.1:c.*625A>C	ENSP00000481634.1:n.*625A>C
NM_001130997.2:c.460A>C	NP_001124469.1:p.Asn154His
NM_152274.4:c.460A>C	NP_689487.2:p.Asn154His
XM_005277920.3:c.430A>C	XP_005277977.1:p.Asn144His
XM_005277921.3:c.430A>C	XP_005277978.1:p.Asn144His
XM_011531213.1:c.334A>C	XP_011529515.1:p.Asn112His
XM_011531214.1:c.334A>C	XP_011529516.1:p.Asn112His
XM_011531215.1:c.334A>C	XP_011529517.1:p.Asn112His
XM_005277920.4:c.430A>C	XP_005277977.1:p.Asn144His
XM_005277921.4:c.430A>C	XP_005277978.1:p.Asn144His
XM_011531214.2:c.334A>C	XP_011529516.1:p.Asn112His
XM_011531215.2:c.334A>C	XP_011529517.1:p.Asn112His
XR_002958810.1:n.2365A>C
NM_152274.5:c.460A>C MANE Select	NP_689487.2:p.Asn154His
NM_001130997.3:c.460A>C	NP_001124469.1:p.Asn154His