Canonical Allele Identifier: CA2795863151
Gene: COL2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47986094_47986095insA , CM000674.2:g.47986094_47986095insA GRCh38
NC_000012.11:g.48379877_48379878insA , CM000674.1:g.48379877_48379878insA GRCh37
NC_000012.10:g.46666144_46666145insA NCBI36
NG_008072.1:g.23408_23409insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000337299.7:c.1321-130_1321-129insT ENSP00000338213.6:n.1321-130_1321-129insT
ENST00000380518.8:c.1528-130_1528-129insT MANE Select ENSP00000369889.3:n.1528-130_1528-129insT
ENST00000337299.6:c.1321-130_1321-129insT ENSP00000338213.6:n.1321-130_1321-129insT
ENST00000380518.7:c.1528-130_1528-129insT ENSP00000369889.3:n.1528-130_1528-129insT
ENST00000493991.5:n.452-130_452-129insT
NM_001844.4:c.1528-130_1528-129insT NP_001835.3:n.1528-130_1528-129insT
NM_033150.2:c.1321-130_1321-129insT NP_149162.2:n.1321-130_1321-129insT
XM_006719242.2:c.1672-130_1672-129insT XP_006719305.2:n.1672-130_1672-129insT
XM_011537928.1:c.1672-130_1672-129insT XP_011536230.1:n.1672-130_1672-129insT
XM_011537929.1:c.1672-130_1672-129insT XP_011536231.1:n.1672-130_1672-129insT
XM_011537930.1:c.1672-130_1672-129insT XP_011536232.1:n.1672-130_1672-129insT
XM_011537931.1:c.1672-130_1672-129insT XP_011536233.1:n.1672-130_1672-129insT
XM_011537932.1:c.1672-130_1672-129insT XP_011536234.1:n.1672-130_1672-129insT
XM_011537933.1:c.1672-130_1672-129insT XP_011536235.1:n.1672-130_1672-129insT
XM_011537934.1:c.1669-130_1669-129insT XP_011536236.1:n.1669-130_1669-129insT
XM_011537935.1:c.616-130_616-129insT XP_011536237.1:n.616-130_616-129insT
XM_017018828.1:c.1672-130_1672-129insT XP_016874317.1:n.1672-130_1672-129insT
XM_017018829.1:c.1669-130_1669-129insT XP_016874318.1:n.1669-130_1669-129insT
XM_017018830.1:c.1462-130_1462-129insT XP_016874319.1:n.1462-130_1462-129insT
XM_017018831.2:c.982-130_982-129insT XP_016874320.1:n.982-130_982-129insT
NM_001844.5:c.1528-130_1528-129insT MANE Select NP_001835.3:n.1528-130_1528-129insT
NM_033150.3:c.1321-130_1321-129insT NP_149162.2:n.1321-130_1321-129insT