Canonical Allele Identifier: CA2795864010

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47977299T>G , CM000674.2:g.47977299T>G	GRCh38
NC_000012.11:g.48371082T>G , CM000674.1:g.48371082T>G	GRCh37
NC_000012.10:g.46657349T>G	NCBI36
NG_008072.1:g.32204A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.3066+21A>C	ENSP00000338213.6:n.3066+21A>C
ENST00000380518.8:c.3273+21A>C MANE Select	ENSP00000369889.3:n.3273+21A>C
ENST00000337299.6:c.3066+21A>C	ENSP00000338213.6:n.3066+21A>C
ENST00000380518.7:c.3273+21A>C	ENSP00000369889.3:n.3273+21A>C
ENST00000493991.5:n.2359+21A>C
ENST00000546974.1:n.126+21A>C
NM_001844.4:c.3273+21A>C	NP_001835.3:n.3273+21A>C
NM_033150.2:c.3066+21A>C	NP_149162.2:n.3066+21A>C
XM_006719242.2:c.3417+21A>C	XP_006719305.2:n.3417+21A>C
XM_011537928.1:c.3417+21A>C	XP_011536230.1:n.3417+21A>C
XM_011537929.1:c.3417+21A>C	XP_011536231.1:n.3417+21A>C
XM_011537930.1:c.3417+21A>C	XP_011536232.1:n.3417+21A>C
XM_011537931.1:c.3417+21A>C	XP_011536233.1:n.3417+21A>C
XM_011537932.1:c.3417+21A>C	XP_011536234.1:n.3417+21A>C
XM_011537933.1:c.3417+21A>C	XP_011536235.1:n.3417+21A>C
XM_011537934.1:c.3414+21A>C	XP_011536236.1:n.3414+21A>C
XM_011537935.1:c.2361+21A>C	XP_011536237.1:n.2361+21A>C
XM_017018828.1:c.3417+21A>C	XP_016874317.1:n.3417+21A>C
XM_017018829.1:c.3414+21A>C	XP_016874318.1:n.3414+21A>C
XM_017018830.1:c.3207+21A>C	XP_016874319.1:n.3207+21A>C
XM_017018831.2:c.2727+21A>C	XP_016874320.1:n.2727+21A>C
NM_001844.5:c.3273+21A>C MANE Select	NP_001835.3:n.3273+21A>C
NM_033150.3:c.3066+21A>C	NP_149162.2:n.3066+21A>C