Canonical Allele Identifier: CA415087210
Gene: CCNQ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153592512C>G , CM000685.2:g.153592512C>G GRCh38
NC_000023.10:g.152857970C>G , CM000685.1:g.152857970C>G GRCh37
NC_000023.9:g.152511164C>G NCBI36
NG_008393.2:g.11666G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000576892.8:c.651G>C MANE Select ENSP00000461135.1:p.Trp217Cys
ENST00000429336.5:c.193+2035G>C
ENST00000440428.5:c.651G>C ENSP00000402949.2:p.Trp217Cys
ENST00000576892.7:c.651G>C ENSP00000461135.1:p.Trp217Cys
ENST00000614850.1:c.277+3492G>C
ENST00000614851.4:c.472G>C
ENST00000620088.4:c.*527G>C ENSP00000484108.1:n.*527G>C
ENST00000621629.4:c.*527G>C ENSP00000478747.1:n.*527G>C
NM_001130997.2:c.651G>C NP_001124469.1:p.Trp217Cys
NM_152274.4:c.651G>C NP_689487.2:p.Trp217Cys
XM_005277920.3:c.621G>C XP_005277977.1:p.Trp207Cys
XM_005277921.3:c.621G>C XP_005277978.1:p.Trp207Cys
XM_011531213.1:c.525G>C XP_011529515.1:p.Trp175Cys
XM_011531214.1:c.525G>C XP_011529516.1:p.Trp175Cys
XM_011531215.1:c.525G>C XP_011529517.1:p.Trp175Cys
XM_005277920.4:c.621G>C XP_005277977.1:p.Trp207Cys
XM_005277921.4:c.621G>C XP_005277978.1:p.Trp207Cys
XM_011531214.2:c.525G>C XP_011529516.1:p.Trp175Cys
XM_011531215.2:c.525G>C XP_011529517.1:p.Trp175Cys
XR_002958810.1:n.2556G>C
NM_152274.5:c.651G>C MANE Select NP_689487.2:p.Trp217Cys
NM_001130997.3:c.651G>C NP_001124469.1:p.Trp217Cys