Canonical Allele Identifier: CA2795861365

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47977849_47977850insAGA , CM000674.2:g.47977849_47977850insAGA	GRCh38
NC_000012.11:g.48371632_48371633insAGA , CM000674.1:g.48371632_48371633insAGA	GRCh37
NC_000012.10:g.46657899_46657900insAGA	NCBI36
NG_008072.1:g.31653_31654insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.2904+160_2904+161insTCT	ENSP00000338213.6:n.2904+160_2904+161insTCT
ENST00000380518.8:c.3111+160_3111+161insTCT MANE Select	ENSP00000369889.3:n.3111+160_3111+161insTCT
ENST00000337299.6:c.2904+160_2904+161insTCT	ENSP00000338213.6:n.2904+160_2904+161insTCT
ENST00000380518.7:c.3111+160_3111+161insTCT	ENSP00000369889.3:n.3111+160_3111+161insTCT
ENST00000493991.5:n.2197+160_2197+161insTCT
NM_001844.4:c.3111+160_3111+161insTCT	NP_001835.3:n.3111+160_3111+161insTCT
NM_033150.2:c.2904+160_2904+161insTCT	NP_149162.2:n.2904+160_2904+161insTCT
XM_006719242.2:c.3255+160_3255+161insTCT	XP_006719305.2:n.3255+160_3255+161insTCT
XM_011537928.1:c.3255+160_3255+161insTCT	XP_011536230.1:n.3255+160_3255+161insTCT
XM_011537929.1:c.3255+160_3255+161insTCT	XP_011536231.1:n.3255+160_3255+161insTCT
XM_011537930.1:c.3255+160_3255+161insTCT	XP_011536232.1:n.3255+160_3255+161insTCT
XM_011537931.1:c.3255+160_3255+161insTCT	XP_011536233.1:n.3255+160_3255+161insTCT
XM_011537932.1:c.3255+160_3255+161insTCT	XP_011536234.1:n.3255+160_3255+161insTCT
XM_011537933.1:c.3255+160_3255+161insTCT	XP_011536235.1:n.3255+160_3255+161insTCT
XM_011537934.1:c.3252+160_3252+161insTCT	XP_011536236.1:n.3252+160_3252+161insTCT
XM_011537935.1:c.2199+160_2199+161insTCT	XP_011536237.1:n.2199+160_2199+161insTCT
XM_017018828.1:c.3255+160_3255+161insTCT	XP_016874317.1:n.3255+160_3255+161insTCT
XM_017018829.1:c.3252+160_3252+161insTCT	XP_016874318.1:n.3252+160_3252+161insTCT
XM_017018830.1:c.3045+160_3045+161insTCT	XP_016874319.1:n.3045+160_3045+161insTCT
XM_017018831.2:c.2565+160_2565+161insTCT	XP_016874320.1:n.2565+160_2565+161insTCT
NM_001844.5:c.3111+160_3111+161insTCT MANE Select	NP_001835.3:n.3111+160_3111+161insTCT
NM_033150.3:c.2904+160_2904+161insTCT	NP_149162.2:n.2904+160_2904+161insTCT