Canonical Allele Identifier: CA384533540
Gene: COL2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47974159G>T , CM000674.2:g.47974159G>T GRCh38
NC_000012.11:g.48367942G>T , CM000674.1:g.48367942G>T GRCh37
NC_000012.10:g.46654209G>T NCBI36
NG_008072.1:g.35344C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000337299.7:c.4040C>A ENSP00000338213.6:p.Ser1347Tyr
ENST00000380518.8:c.4247C>A MANE Select ENSP00000369889.3:p.Ser1416Tyr
ENST00000337299.6:c.4040C>A ENSP00000338213.6:p.Ser1347Tyr
ENST00000380518.7:c.4247C>A ENSP00000369889.3:p.Ser1416Tyr
ENST00000493991.5:n.3333C>A
NM_001844.4:c.4247C>A NP_001835.3:p.Ser1416Tyr
NM_033150.2:c.4040C>A NP_149162.2:p.Ser1347Tyr
XM_006719242.2:c.4391C>A XP_006719305.2:p.Ser1464Tyr
XM_011537928.1:c.4391C>A XP_011536230.1:p.Ser1464Tyr
XM_011537929.1:c.4391C>A XP_011536231.1:p.Ser1464Tyr
XM_011537930.1:c.4391C>A XP_011536232.1:p.Ser1464Tyr
XM_011537931.1:c.4391C>A XP_011536233.1:p.Ser1464Tyr
XM_011537932.1:c.4391C>A XP_011536234.1:p.Ser1464Tyr
XM_011537933.1:c.4391C>A XP_011536235.1:p.Ser1464Tyr
XM_011537934.1:c.4388C>A XP_011536236.1:p.Ser1463Tyr
XM_011537935.1:c.3335C>A XP_011536237.1:p.Ser1112Tyr
XM_017018828.1:c.4391C>A XP_016874317.1:p.Ser1464Tyr
XM_017018829.1:c.4388C>A XP_016874318.1:p.Ser1463Tyr
XM_017018830.1:c.4181C>A XP_016874319.1:p.Ser1394Tyr
XM_017018831.2:c.3701C>A XP_016874320.1:p.Ser1234Tyr
NM_001844.5:c.4247C>A MANE Select NP_001835.3:p.Ser1416Tyr
NM_033150.3:c.4040C>A NP_149162.2:p.Ser1347Tyr