Canonical Allele Identifier: CA2695216645
Gene: COL2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47978100dup , CM000674.2:g.47978100dup GRCh38
NC_000012.11:g.48371883dup , CM000674.1:g.48371883dup GRCh37
NC_000012.10:g.46658150dup NCBI36
NG_008072.1:g.31405dup

Transcript Alleles

HGVS Amino-acid change
ENST00000337299.7:c.2816dup ENSP00000338213.6:p.Ala940CysfsTer25
ENST00000380518.8:c.3023dup MANE Select ENSP00000369889.3:p.Ala1009CysfsTer25
ENST00000337299.6:c.2816dup ENSP00000338213.6:p.Ala940CysfsTer25
ENST00000380518.7:c.3023dup ENSP00000369889.3:p.Ala1009CysfsTer25
ENST00000493991.5:n.2109dup
NM_001844.4:c.3023dup NP_001835.3:p.Ala1009CysfsTer25
NM_033150.2:c.2816dup NP_149162.2:p.Ala940CysfsTer25
XM_006719242.2:c.3167dup XP_006719305.2:p.Ala1057CysfsTer25
XM_011537928.1:c.3167dup XP_011536230.1:p.Ala1057CysfsTer25
XM_011537929.1:c.3167dup XP_011536231.1:p.Ala1057CysfsTer25
XM_011537930.1:c.3167dup XP_011536232.1:p.Ala1057CysfsTer25
XM_011537931.1:c.3167dup XP_011536233.1:p.Ala1057CysfsTer25
XM_011537932.1:c.3167dup XP_011536234.1:p.Ala1057CysfsTer25
XM_011537933.1:c.3167dup XP_011536235.1:p.Ala1057CysfsTer25
XM_011537934.1:c.3164dup XP_011536236.1:p.Ala1056CysfsTer25
XM_011537935.1:c.2111dup XP_011536237.1:p.Ala705CysfsTer25
XM_017018828.1:c.3167dup XP_016874317.1:p.Ala1057CysfsTer25
XM_017018829.1:c.3164dup XP_016874318.1:p.Ala1056CysfsTer25
XM_017018830.1:c.2957dup XP_016874319.1:p.Ala987CysfsTer25
XM_017018831.2:c.2477dup XP_016874320.1:p.Ala827CysfsTer25
NM_001844.5:c.3023dup MANE Select NP_001835.3:p.Ala1009CysfsTer25
NM_033150.3:c.2816dup NP_149162.2:p.Ala940CysfsTer25