Canonical Allele Identifier: CA384526713
Gene: COL2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48000096G>T , CM000674.2:g.48000096G>T GRCh38
NC_000012.11:g.48393879G>T , CM000674.1:g.48393879G>T GRCh37
NC_000012.10:g.46680146G>T NCBI36
NG_008072.1:g.9407C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000337299.7:c.86-1665C>A ENSP00000338213.6:n.86-1665C>A
ENST00000380518.8:c.115C>A MANE Select ENSP00000369889.3:p.Gln39Lys
ENST00000490609.2:n.348C>A
ENST00000337299.6:c.86-1665C>A ENSP00000338213.6:n.86-1665C>A
ENST00000380518.7:c.115C>A ENSP00000369889.3:p.Gln39Lys
ENST00000474996.6:n.353C>A
ENST00000490609.1:n.280C>A
NM_001844.4:c.115C>A NP_001835.3:p.Gln39Lys
NM_033150.2:c.86-1665C>A NP_149162.2:n.86-1665C>A
XM_006719242.2:c.256C>A XP_006719305.2:p.Gln86Lys
XM_011537928.1:c.256C>A XP_011536230.1:p.Gln86Lys
XM_011537929.1:c.256C>A XP_011536231.1:p.Gln86Lys
XM_011537930.1:c.256C>A XP_011536232.1:p.Gln86Lys
XM_011537931.1:c.256C>A XP_011536233.1:p.Gln86Lys
XM_011537932.1:c.256C>A XP_011536234.1:p.Gln86Lys
XM_011537933.1:c.256C>A XP_011536235.1:p.Gln86Lys
XM_011537934.1:c.256C>A XP_011536236.1:p.Gln86Lys
XM_017018828.1:c.256C>A XP_016874317.1:p.Gln86Lys
XM_017018829.1:c.256C>A XP_016874318.1:p.Gln86Lys
XM_017018830.1:c.227-1665C>A XP_016874319.1:n.227-1665C>A
XM_017018831.2:c.-432C>A XP_016874320.1:n.-432C>A
NM_001844.5:c.115C>A MANE Select NP_001835.3:p.Gln39Lys
NM_033150.3:c.86-1665C>A NP_149162.2:n.86-1665C>A