Canonical Allele Identifier: CA2529301832
Gene: COL2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2137327
ClinVar RCV Id: RCV003062493

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47977633dup , CM000674.2:g.47977633dup GRCh38
NC_000012.11:g.48371416dup , CM000674.1:g.48371416dup GRCh37
NC_000012.10:g.46657683dup NCBI36
NG_008072.1:g.31875dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000337299.7:c.2930dup ENSP00000338213.6:p.Gly978TrpfsTer11
ENST00000380518.8:c.3137dup MANE Select ENSP00000369889.3:p.Gly1047TrpfsTer11
ENST00000337299.6:c.2930dup ENSP00000338213.6:p.Gly978TrpfsTer11
ENST00000380518.7:c.3137dup ENSP00000369889.3:p.Gly1047TrpfsTer11
ENST00000493991.5:n.2223dup
NM_001844.4:c.3137dup NP_001835.3:p.Gly1047TrpfsTer11
NM_033150.2:c.2930dup NP_149162.2:p.Gly978TrpfsTer11
XM_006719242.2:c.3281dup XP_006719305.2:p.Gly1095TrpfsTer11
XM_011537928.1:c.3281dup XP_011536230.1:p.Gly1095TrpfsTer11
XM_011537929.1:c.3281dup XP_011536231.1:p.Gly1095TrpfsTer11
XM_011537930.1:c.3281dup XP_011536232.1:p.Gly1095TrpfsTer11
XM_011537931.1:c.3281dup XP_011536233.1:p.Gly1095TrpfsTer11
XM_011537932.1:c.3281dup XP_011536234.1:p.Gly1095TrpfsTer11
XM_011537933.1:c.3281dup XP_011536235.1:p.Gly1095TrpfsTer11
XM_011537934.1:c.3278dup XP_011536236.1:p.Gly1094TrpfsTer11
XM_011537935.1:c.2225dup XP_011536237.1:p.Gly743TrpfsTer11
XM_017018828.1:c.3281dup XP_016874317.1:p.Gly1095TrpfsTer11
XM_017018829.1:c.3278dup XP_016874318.1:p.Gly1094TrpfsTer11
XM_017018830.1:c.3071dup XP_016874319.1:p.Gly1025TrpfsTer11
XM_017018831.2:c.2591dup XP_016874320.1:p.Gly865TrpfsTer11
NM_001844.5:c.3137dup MANE Select NP_001835.3:p.Gly1047TrpfsTer11
NM_033150.3:c.2930dup NP_149162.2:p.Gly978TrpfsTer11