Canonical Allele Identifier: CA2795863047

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47985966_47985967insAG , CM000674.2:g.47985966_47985967insAG	GRCh38
NC_000012.11:g.48379749_48379750insAG , CM000674.1:g.48379749_48379750insAG	GRCh37
NC_000012.10:g.46666016_46666017insAG	NCBI36
NG_008072.1:g.23536_23537insCT

Transcript Alleles

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