Canonical Allele Identifier: CA2618507506
Gene: COL2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47989106_47989113del , CM000674.2:g.47989106_47989113del GRCh38
NC_000012.11:g.48382889_48382896del , CM000674.1:g.48382889_48382896del GRCh37
NC_000012.10:g.46669156_46669163del NCBI36
NG_008072.1:g.20397_20404del

Transcript Alleles

HGVS Amino-acid Change
ENST00000337299.7:c.915+122_915+129del ENSP00000338213.6:n.915+122_915+129del
ENST00000380518.8:c.1122+122_1122+129del MANE Select ENSP00000369889.3:n.1122+122_1122+129del
ENST00000337299.6:c.915+122_915+129del ENSP00000338213.6:n.915+122_915+129del
ENST00000380518.7:c.1122+122_1122+129del ENSP00000369889.3:n.1122+122_1122+129del
NM_001844.4:c.1122+122_1122+129del NP_001835.3:n.1122+122_1122+129del
NM_033150.2:c.915+122_915+129del NP_149162.2:n.915+122_915+129del
XM_006719242.2:c.1266+122_1266+129del XP_006719305.2:n.1266+122_1266+129del
XM_011537928.1:c.1266+122_1266+129del XP_011536230.1:n.1266+122_1266+129del
XM_011537929.1:c.1266+122_1266+129del XP_011536231.1:n.1266+122_1266+129del
XM_011537930.1:c.1266+122_1266+129del XP_011536232.1:n.1266+122_1266+129del
XM_011537931.1:c.1266+122_1266+129del XP_011536233.1:n.1266+122_1266+129del
XM_011537932.1:c.1266+122_1266+129del XP_011536234.1:n.1266+122_1266+129del
XM_011537933.1:c.1266+122_1266+129del XP_011536235.1:n.1266+122_1266+129del
XM_011537934.1:c.1263+122_1263+129del XP_011536236.1:n.1263+122_1263+129del
XM_017018828.1:c.1266+122_1266+129del XP_016874317.1:n.1266+122_1266+129del
XM_017018829.1:c.1263+122_1263+129del XP_016874318.1:n.1263+122_1263+129del
XM_017018830.1:c.1056+122_1056+129del XP_016874319.1:n.1056+122_1056+129del
XM_017018831.2:c.576+122_576+129del XP_016874320.1:n.576+122_576+129del
NM_001844.5:c.1122+122_1122+129del MANE Select NP_001835.3:n.1122+122_1122+129del
NM_033150.3:c.915+122_915+129del NP_149162.2:n.915+122_915+129del