Canonical Allele Identifier: CA2795863221

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47993568_47993569del , CM000674.2:g.47993568_47993569del	GRCh38
NC_000012.11:g.48387351_48387352del , CM000674.1:g.48387351_48387352del	GRCh37
NC_000012.10:g.46673618_46673619del	NCBI36
NG_008072.1:g.15934_15935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.718-67_718-66del	ENSP00000338213.6:n.718-67_718-66del
ENST00000380518.8:c.925-67_925-66del MANE Select	ENSP00000369889.3:n.925-67_925-66del
ENST00000337299.6:c.718-67_718-66del	ENSP00000338213.6:n.718-67_718-66del
ENST00000380518.7:c.925-67_925-66del	ENSP00000369889.3:n.925-67_925-66del
NM_001844.4:c.925-67_925-66del	NP_001835.3:n.925-67_925-66del
NM_033150.2:c.718-67_718-66del	NP_149162.2:n.718-67_718-66del
XM_006719242.2:c.1069-67_1069-66del	XP_006719305.2:n.1069-67_1069-66del
XM_011537928.1:c.1069-67_1069-66del	XP_011536230.1:n.1069-67_1069-66del
XM_011537929.1:c.1069-67_1069-66del	XP_011536231.1:n.1069-67_1069-66del
XM_011537930.1:c.1069-67_1069-66del	XP_011536232.1:n.1069-67_1069-66del
XM_011537931.1:c.1069-67_1069-66del	XP_011536233.1:n.1069-67_1069-66del
XM_011537932.1:c.1069-67_1069-66del	XP_011536234.1:n.1069-67_1069-66del
XM_011537933.1:c.1069-67_1069-66del	XP_011536235.1:n.1069-67_1069-66del
XM_011537934.1:c.1066-67_1066-66del	XP_011536236.1:n.1066-67_1066-66del
XM_017018828.1:c.1069-67_1069-66del	XP_016874317.1:n.1069-67_1069-66del
XM_017018829.1:c.1066-67_1066-66del	XP_016874318.1:n.1066-67_1066-66del
XM_017018830.1:c.859-67_859-66del	XP_016874319.1:n.859-67_859-66del
XM_017018831.2:c.379-67_379-66del	XP_016874320.1:n.379-67_379-66del
NM_001844.5:c.925-67_925-66del MANE Select	NP_001835.3:n.925-67_925-66del
NM_033150.3:c.718-67_718-66del	NP_149162.2:n.718-67_718-66del