Canonical Allele Identifier: CA2034461403
Gene: COL2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47989258A= , CM000674.2:g.47989258A= GRCh38
NC_000012.11:g.48383041A= , CM000674.1:g.48383041A= GRCh37
NC_000012.10:g.46669308A= NCBI36
NG_008072.1:g.20245T=

Transcript Alleles

HGVS Amino-acid change
ENST00000337299.7:c.885T= ENSP00000338213.6:p.Gly295=
ENST00000380518.8:c.1092T= MANE Select ENSP00000369889.3:p.Gly364=
ENST00000337299.6:c.885T= ENSP00000338213.6:p.Gly295=
ENST00000380518.7:c.1092T= ENSP00000369889.3:p.Gly364=
NM_001844.4:c.1092T= NP_001835.3:p.Gly364=
NM_033150.2:c.885T= NP_149162.2:p.Gly295=
XM_006719242.2:c.1236T= XP_006719305.2:p.Gly412=
XM_011537928.1:c.1236T= XP_011536230.1:p.Gly412=
XM_011537929.1:c.1236T= XP_011536231.1:p.Gly412=
XM_011537930.1:c.1236T= XP_011536232.1:p.Gly412=
XM_011537931.1:c.1236T= XP_011536233.1:p.Gly412=
XM_011537932.1:c.1236T= XP_011536234.1:p.Gly412=
XM_011537933.1:c.1236T= XP_011536235.1:p.Gly412=
XM_011537934.1:c.1233T= XP_011536236.1:p.Gly411=
XM_017018828.1:c.1236T= XP_016874317.1:p.Gly412=
XM_017018829.1:c.1233T= XP_016874318.1:p.Gly411=
XM_017018830.1:c.1026T= XP_016874319.1:p.Gly342=
XM_017018831.2:c.546T= XP_016874320.1:p.Gly182=
NM_001844.5:c.1092T= MANE Select NP_001835.3:p.Gly364=
NM_033150.3:c.885T= NP_149162.2:p.Gly295=