Canonical Allele Identifier: CA384526432
Gene: COL2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48000048A>C , CM000674.2:g.48000048A>C GRCh38
NC_000012.11:g.48393831A>C , CM000674.1:g.48393831A>C GRCh37
NC_000012.10:g.46680098A>C NCBI36
NG_008072.1:g.9455T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000337299.7:c.86-1617T>G ENSP00000338213.6:n.86-1617T>G
ENST00000380518.8:c.163T>G MANE Select ENSP00000369889.3:p.Cys55Gly
ENST00000490609.2:n.396T>G
ENST00000337299.6:c.86-1617T>G ENSP00000338213.6:n.86-1617T>G
ENST00000380518.7:c.163T>G ENSP00000369889.3:p.Cys55Gly
ENST00000474996.6:n.401T>G
ENST00000490609.1:n.328T>G
NM_001844.4:c.163T>G NP_001835.3:p.Cys55Gly
NM_033150.2:c.86-1617T>G NP_149162.2:n.86-1617T>G
XM_006719242.2:c.304T>G XP_006719305.2:p.Cys102Gly
XM_011537928.1:c.304T>G XP_011536230.1:p.Cys102Gly
XM_011537929.1:c.304T>G XP_011536231.1:p.Cys102Gly
XM_011537930.1:c.304T>G XP_011536232.1:p.Cys102Gly
XM_011537931.1:c.304T>G XP_011536233.1:p.Cys102Gly
XM_011537932.1:c.304T>G XP_011536234.1:p.Cys102Gly
XM_011537933.1:c.304T>G XP_011536235.1:p.Cys102Gly
XM_011537934.1:c.304T>G XP_011536236.1:p.Cys102Gly
XM_017018828.1:c.304T>G XP_016874317.1:p.Cys102Gly
XM_017018829.1:c.304T>G XP_016874318.1:p.Cys102Gly
XM_017018830.1:c.227-1617T>G XP_016874319.1:n.227-1617T>G
XM_017018831.2:c.-384T>G XP_016874320.1:n.-384T>G
NM_001844.5:c.163T>G MANE Select NP_001835.3:p.Cys55Gly
NM_033150.3:c.86-1617T>G NP_149162.2:n.86-1617T>G