Canonical Allele Identifier: CA2838415822

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47977225dup , CM000674.2:g.47977225dup	GRCh38
NC_000012.11:g.48371008dup , CM000674.1:g.48371008dup	GRCh37
NC_000012.10:g.46657275dup	NCBI36
NG_008072.1:g.32279dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.3067-69dup	ENSP00000338213.6:n.3067-69dup
ENST00000380518.8:c.3274-69dup MANE Select	ENSP00000369889.3:n.3274-69dup
ENST00000337299.6:c.3067-69dup	ENSP00000338213.6:n.3067-69dup
ENST00000380518.7:c.3274-69dup	ENSP00000369889.3:n.3274-69dup
ENST00000493991.5:n.2360-69dup
ENST00000546974.1:n.127-69dup
NM_001844.4:c.3274-69dup	NP_001835.3:n.3274-69dup
NM_033150.2:c.3067-69dup	NP_149162.2:n.3067-69dup
XM_006719242.2:c.3418-69dup	XP_006719305.2:n.3418-69dup
XM_011537928.1:c.3418-69dup	XP_011536230.1:n.3418-69dup
XM_011537929.1:c.3418-69dup	XP_011536231.1:n.3418-69dup
XM_011537930.1:c.3418-69dup	XP_011536232.1:n.3418-69dup
XM_011537931.1:c.3418-69dup	XP_011536233.1:n.3418-69dup
XM_011537932.1:c.3418-69dup	XP_011536234.1:n.3418-69dup
XM_011537933.1:c.3418-69dup	XP_011536235.1:n.3418-69dup
XM_011537934.1:c.3415-69dup	XP_011536236.1:n.3415-69dup
XM_011537935.1:c.2362-69dup	XP_011536237.1:n.2362-69dup
XM_017018828.1:c.3418-69dup	XP_016874317.1:n.3418-69dup
XM_017018829.1:c.3415-69dup	XP_016874318.1:n.3415-69dup
XM_017018830.1:c.3208-69dup	XP_016874319.1:n.3208-69dup
XM_017018831.2:c.2728-69dup	XP_016874320.1:n.2728-69dup
NM_001844.5:c.3274-69dup MANE Select	NP_001835.3:n.3274-69dup
NM_033150.3:c.3067-69dup	NP_149162.2:n.3067-69dup