Canonical Allele Identifier: CA2795863994

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47977281_47977282insAGA , CM000674.2:g.47977281_47977282insAGA	GRCh38
NC_000012.11:g.48371064_48371065insAGA , CM000674.1:g.48371064_48371065insAGA	GRCh37
NC_000012.10:g.46657331_46657332insAGA	NCBI36
NG_008072.1:g.32221_32222insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.3066+38_3066+39insTCT	ENSP00000338213.6:n.3066+38_3066+39insTCT
ENST00000380518.8:c.3273+38_3273+39insTCT MANE Select	ENSP00000369889.3:n.3273+38_3273+39insTCT
ENST00000337299.6:c.3066+38_3066+39insTCT	ENSP00000338213.6:n.3066+38_3066+39insTCT
ENST00000380518.7:c.3273+38_3273+39insTCT	ENSP00000369889.3:n.3273+38_3273+39insTCT
ENST00000493991.5:n.2359+38_2359+39insTCT
ENST00000546974.1:n.126+38_126+39insTCT
NM_001844.4:c.3273+38_3273+39insTCT	NP_001835.3:n.3273+38_3273+39insTCT
NM_033150.2:c.3066+38_3066+39insTCT	NP_149162.2:n.3066+38_3066+39insTCT
XM_006719242.2:c.3417+38_3417+39insTCT	XP_006719305.2:n.3417+38_3417+39insTCT
XM_011537928.1:c.3417+38_3417+39insTCT	XP_011536230.1:n.3417+38_3417+39insTCT
XM_011537929.1:c.3417+38_3417+39insTCT	XP_011536231.1:n.3417+38_3417+39insTCT
XM_011537930.1:c.3417+38_3417+39insTCT	XP_011536232.1:n.3417+38_3417+39insTCT
XM_011537931.1:c.3417+38_3417+39insTCT	XP_011536233.1:n.3417+38_3417+39insTCT
XM_011537932.1:c.3417+38_3417+39insTCT	XP_011536234.1:n.3417+38_3417+39insTCT
XM_011537933.1:c.3417+38_3417+39insTCT	XP_011536235.1:n.3417+38_3417+39insTCT
XM_011537934.1:c.3414+38_3414+39insTCT	XP_011536236.1:n.3414+38_3414+39insTCT
XM_011537935.1:c.2361+38_2361+39insTCT	XP_011536237.1:n.2361+38_2361+39insTCT
XM_017018828.1:c.3417+38_3417+39insTCT	XP_016874317.1:n.3417+38_3417+39insTCT
XM_017018829.1:c.3414+38_3414+39insTCT	XP_016874318.1:n.3414+38_3414+39insTCT
XM_017018830.1:c.3207+38_3207+39insTCT	XP_016874319.1:n.3207+38_3207+39insTCT
XM_017018831.2:c.2727+38_2727+39insTCT	XP_016874320.1:n.2727+38_2727+39insTCT
NM_001844.5:c.3273+38_3273+39insTCT MANE Select	NP_001835.3:n.3273+38_3273+39insTCT
NM_033150.3:c.3066+38_3066+39insTCT	NP_149162.2:n.3066+38_3066+39insTCT