Canonical Allele Identifier: CA2795863276

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47993595_47993596insCAG , CM000674.2:g.47993595_47993596insCAG	GRCh38
NC_000012.11:g.48387378_48387379insCAG , CM000674.1:g.48387378_48387379insCAG	GRCh37
NC_000012.10:g.46673645_46673646insCAG	NCBI36
NG_008072.1:g.15907_15908insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.718-94_718-93insCTG	ENSP00000338213.6:n.718-94_718-93insCTG
ENST00000380518.8:c.925-94_925-93insCTG MANE Select	ENSP00000369889.3:n.925-94_925-93insCTG
ENST00000337299.6:c.718-94_718-93insCTG	ENSP00000338213.6:n.718-94_718-93insCTG
ENST00000380518.7:c.925-94_925-93insCTG	ENSP00000369889.3:n.925-94_925-93insCTG
NM_001844.4:c.925-94_925-93insCTG	NP_001835.3:n.925-94_925-93insCTG
NM_033150.2:c.718-94_718-93insCTG	NP_149162.2:n.718-94_718-93insCTG
XM_006719242.2:c.1069-94_1069-93insCTG	XP_006719305.2:n.1069-94_1069-93insCTG
XM_011537928.1:c.1069-94_1069-93insCTG	XP_011536230.1:n.1069-94_1069-93insCTG
XM_011537929.1:c.1069-94_1069-93insCTG	XP_011536231.1:n.1069-94_1069-93insCTG
XM_011537930.1:c.1069-94_1069-93insCTG	XP_011536232.1:n.1069-94_1069-93insCTG
XM_011537931.1:c.1069-94_1069-93insCTG	XP_011536233.1:n.1069-94_1069-93insCTG
XM_011537932.1:c.1069-94_1069-93insCTG	XP_011536234.1:n.1069-94_1069-93insCTG
XM_011537933.1:c.1069-94_1069-93insCTG	XP_011536235.1:n.1069-94_1069-93insCTG
XM_011537934.1:c.1066-94_1066-93insCTG	XP_011536236.1:n.1066-94_1066-93insCTG
XM_017018828.1:c.1069-94_1069-93insCTG	XP_016874317.1:n.1069-94_1069-93insCTG
XM_017018829.1:c.1066-94_1066-93insCTG	XP_016874318.1:n.1066-94_1066-93insCTG
XM_017018830.1:c.859-94_859-93insCTG	XP_016874319.1:n.859-94_859-93insCTG
XM_017018831.2:c.379-94_379-93insCTG	XP_016874320.1:n.379-94_379-93insCTG
NM_001844.5:c.925-94_925-93insCTG MANE Select	NP_001835.3:n.925-94_925-93insCTG
NM_033150.3:c.718-94_718-93insCTG	NP_149162.2:n.718-94_718-93insCTG