Canonical Allele Identifier: CA2575138416

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47993544_47993546del , CM000674.2:g.47993544_47993546del	GRCh38
NC_000012.11:g.48387327_48387329del , CM000674.1:g.48387327_48387329del	GRCh37
NC_000012.10:g.46673594_46673596del	NCBI36
NG_008072.1:g.15959_15961del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.718-42_718-40del	ENSP00000338213.6:n.718-42_718-40del
ENST00000380518.8:c.925-42_925-40del MANE Select	ENSP00000369889.3:n.925-42_925-40del
ENST00000337299.6:c.718-42_718-40del	ENSP00000338213.6:n.718-42_718-40del
ENST00000380518.7:c.925-42_925-40del	ENSP00000369889.3:n.925-42_925-40del
NM_001844.4:c.925-42_925-40del	NP_001835.3:n.925-42_925-40del
NM_033150.2:c.718-42_718-40del	NP_149162.2:n.718-42_718-40del
XM_006719242.2:c.1069-42_1069-40del	XP_006719305.2:n.1069-42_1069-40del
XM_011537928.1:c.1069-42_1069-40del	XP_011536230.1:n.1069-42_1069-40del
XM_011537929.1:c.1069-42_1069-40del	XP_011536231.1:n.1069-42_1069-40del
XM_011537930.1:c.1069-42_1069-40del	XP_011536232.1:n.1069-42_1069-40del
XM_011537931.1:c.1069-42_1069-40del	XP_011536233.1:n.1069-42_1069-40del
XM_011537932.1:c.1069-42_1069-40del	XP_011536234.1:n.1069-42_1069-40del
XM_011537933.1:c.1069-42_1069-40del	XP_011536235.1:n.1069-42_1069-40del
XM_011537934.1:c.1066-42_1066-40del	XP_011536236.1:n.1066-42_1066-40del
XM_017018828.1:c.1069-42_1069-40del	XP_016874317.1:n.1069-42_1069-40del
XM_017018829.1:c.1066-42_1066-40del	XP_016874318.1:n.1066-42_1066-40del
XM_017018830.1:c.859-42_859-40del	XP_016874319.1:n.859-42_859-40del
XM_017018831.2:c.379-42_379-40del	XP_016874320.1:n.379-42_379-40del
NM_001844.5:c.925-42_925-40del MANE Select	NP_001835.3:n.925-42_925-40del
NM_033150.3:c.718-42_718-40del	NP_149162.2:n.718-42_718-40del