Canonical Allele Identifier: CA384551537
Gene: COL2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47985767G>T , CM000674.2:g.47985767G>T GRCh38
NC_000012.11:g.48379550G>T , CM000674.1:g.48379550G>T GRCh37
NC_000012.10:g.46665817G>T NCBI36
NG_008072.1:g.23736C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000337299.7:c.1434C>A ENSP00000338213.6:p.Asp478Glu
ENST00000380518.8:c.1641C>A MANE Select ENSP00000369889.3:p.Asp547Glu
ENST00000337299.6:c.1434C>A ENSP00000338213.6:p.Asp478Glu
ENST00000380518.7:c.1641C>A ENSP00000369889.3:p.Asp547Glu
ENST00000493991.5:n.565C>A
NM_001844.4:c.1641C>A NP_001835.3:p.Asp547Glu
NM_033150.2:c.1434C>A NP_149162.2:p.Asp478Glu
XM_006719242.2:c.1785C>A XP_006719305.2:p.Asp595Glu
XM_011537928.1:c.1785C>A XP_011536230.1:p.Asp595Glu
XM_011537929.1:c.1785C>A XP_011536231.1:p.Asp595Glu
XM_011537930.1:c.1785C>A XP_011536232.1:p.Asp595Glu
XM_011537931.1:c.1785C>A XP_011536233.1:p.Asp595Glu
XM_011537932.1:c.1785C>A XP_011536234.1:p.Asp595Glu
XM_011537933.1:c.1785C>A XP_011536235.1:p.Asp595Glu
XM_011537934.1:c.1782C>A XP_011536236.1:p.Asp594Glu
XM_011537935.1:c.729C>A XP_011536237.1:p.Asp243Glu
XM_017018828.1:c.1785C>A XP_016874317.1:p.Asp595Glu
XM_017018829.1:c.1782C>A XP_016874318.1:p.Asp594Glu
XM_017018830.1:c.1575C>A XP_016874319.1:p.Asp525Glu
XM_017018831.2:c.1095C>A XP_016874320.1:p.Asp365Glu
NM_001844.5:c.1641C>A MANE Select NP_001835.3:p.Asp547Glu
NM_033150.3:c.1434C>A NP_149162.2:p.Asp478Glu