Canonical Allele Identifier: CA2034474258

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47975575G= , CM000674.2:g.47975575G=	GRCh38
NC_000012.11:g.48369358G= , CM000674.1:g.48369358G=	GRCh37
NC_000012.10:g.46655625G=	NCBI36
NG_008072.1:g.33928C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.3421C=	ENSP00000338213.6:p.Pro1141=
ENST00000380518.8:c.3628C= MANE Select	ENSP00000369889.3:p.Pro1210=
ENST00000337299.6:c.3421C=	ENSP00000338213.6:p.Pro1141=
ENST00000380518.7:c.3628C=	ENSP00000369889.3:p.Pro1210=
ENST00000493991.5:n.2714C=
ENST00000546974.1:n.481C=
NM_001844.4:c.3628C=	NP_001835.3:p.Pro1210=
NM_033150.2:c.3421C=	NP_149162.2:p.Pro1141=
XM_006719242.2:c.3772C=	XP_006719305.2:p.Pro1258=
XM_011537928.1:c.3772C=	XP_011536230.1:p.Pro1258=
XM_011537929.1:c.3772C=	XP_011536231.1:p.Pro1258=
XM_011537930.1:c.3772C=	XP_011536232.1:p.Pro1258=
XM_011537931.1:c.3772C=	XP_011536233.1:p.Pro1258=
XM_011537932.1:c.3772C=	XP_011536234.1:p.Pro1258=
XM_011537933.1:c.3772C=	XP_011536235.1:p.Pro1258=
XM_011537934.1:c.3769C=	XP_011536236.1:p.Pro1257=
XM_011537935.1:c.2716C=	XP_011536237.1:p.Pro906=
XM_017018828.1:c.3772C=	XP_016874317.1:p.Pro1258=
XM_017018829.1:c.3769C=	XP_016874318.1:p.Pro1257=
XM_017018830.1:c.3562C=	XP_016874319.1:p.Pro1188=
XM_017018831.2:c.3082C=	XP_016874320.1:p.Pro1028=
NM_001844.5:c.3628C= MANE Select	NP_001835.3:p.Pro1210=
NM_033150.3:c.3421C=	NP_149162.2:p.Pro1141=