Canonical Allele Identifier: CA2544583951

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47995804_47995805insCTGG , CM000674.2:g.47995804_47995805insCTGG	GRCh38
NC_000012.11:g.48389587_48389588insCTGG , CM000674.1:g.48389587_48389588insCTGG	GRCh37
NC_000012.10:g.46675854_46675855insCTGG	NCBI36
NG_008072.1:g.13698_13699insCCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.448-42_448-41insCCAG	ENSP00000338213.6:n.448-42_448-41insCCAG
ENST00000380518.8:c.655-42_655-41insCCAG MANE Select	ENSP00000369889.3:n.655-42_655-41insCCAG
ENST00000337299.6:c.448-42_448-41insCCAG	ENSP00000338213.6:n.448-42_448-41insCCAG
ENST00000380518.7:c.655-42_655-41insCCAG	ENSP00000369889.3:n.655-42_655-41insCCAG
NM_001844.4:c.655-42_655-41insCCAG	NP_001835.3:n.655-42_655-41insCCAG
NM_033150.2:c.448-42_448-41insCCAG	NP_149162.2:n.448-42_448-41insCCAG
XM_006719242.2:c.799-42_799-41insCCAG	XP_006719305.2:n.799-42_799-41insCCAG
XM_011537928.1:c.799-42_799-41insCCAG	XP_011536230.1:n.799-42_799-41insCCAG
XM_011537929.1:c.799-42_799-41insCCAG	XP_011536231.1:n.799-42_799-41insCCAG
XM_011537930.1:c.799-42_799-41insCCAG	XP_011536232.1:n.799-42_799-41insCCAG
XM_011537931.1:c.799-42_799-41insCCAG	XP_011536233.1:n.799-42_799-41insCCAG
XM_011537932.1:c.799-42_799-41insCCAG	XP_011536234.1:n.799-42_799-41insCCAG
XM_011537933.1:c.799-42_799-41insCCAG	XP_011536235.1:n.799-42_799-41insCCAG
XM_011537934.1:c.796-42_796-41insCCAG	XP_011536236.1:n.796-42_796-41insCCAG
XM_017018828.1:c.799-42_799-41insCCAG	XP_016874317.1:n.799-42_799-41insCCAG
XM_017018829.1:c.796-42_796-41insCCAG	XP_016874318.1:n.796-42_796-41insCCAG
XM_017018830.1:c.589-42_589-41insCCAG	XP_016874319.1:n.589-42_589-41insCCAG
XM_017018831.2:c.109-42_109-41insCCAG	XP_016874320.1:n.109-42_109-41insCCAG
NM_001844.5:c.655-42_655-41insCCAG MANE Select	NP_001835.3:n.655-42_655-41insCCAG
NM_033150.3:c.448-42_448-41insCCAG	NP_149162.2:n.448-42_448-41insCCAG