Canonical Allele Identifier: CA2034489092
Gene: COL2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47999945C= , CM000674.2:g.47999945C= GRCh38
NC_000012.11:g.48393728C= , CM000674.1:g.48393728C= GRCh37
NC_000012.10:g.46679995C= NCBI36
NG_008072.1:g.9558G=

Transcript Alleles

HGVS Amino-acid change
ENST00000337299.7:c.86-1514G= ENSP00000338213.6:n.86-1514G=
ENST00000380518.8:c.266G= MANE Select ENSP00000369889.3:p.Cys89=
ENST00000490609.2:n.499G=
ENST00000337299.6:c.86-1514G= ENSP00000338213.6:n.86-1514G=
ENST00000380518.7:c.266G= ENSP00000369889.3:p.Cys89=
ENST00000474996.6:n.504G=
ENST00000490609.1:n.431G=
NM_001844.4:c.266G= NP_001835.3:p.Cys89=
NM_033150.2:c.86-1514G= NP_149162.2:n.86-1514G=
XM_006719242.2:c.407G= XP_006719305.2:p.Cys136=
XM_011537928.1:c.407G= XP_011536230.1:p.Cys136=
XM_011537929.1:c.407G= XP_011536231.1:p.Cys136=
XM_011537930.1:c.407G= XP_011536232.1:p.Cys136=
XM_011537931.1:c.407G= XP_011536233.1:p.Cys136=
XM_011537932.1:c.407G= XP_011536234.1:p.Cys136=
XM_011537933.1:c.407G= XP_011536235.1:p.Cys136=
XM_011537934.1:c.407G= XP_011536236.1:p.Cys136=
XM_017018828.1:c.407G= XP_016874317.1:p.Cys136=
XM_017018829.1:c.407G= XP_016874318.1:p.Cys136=
XM_017018830.1:c.227-1514G= XP_016874319.1:n.227-1514G=
XM_017018831.2:c.-281G= XP_016874320.1:n.-281G=
NM_001844.5:c.266G= MANE Select NP_001835.3:p.Cys89=
NM_033150.3:c.86-1514G= NP_149162.2:n.86-1514G=