Canonical Allele Identifier: CA2034474311

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47975599G= , CM000674.2:g.47975599G=	GRCh38
NC_000012.11:g.48369382G= , CM000674.1:g.48369382G=	GRCh37
NC_000012.10:g.46655649G=	NCBI36
NG_008072.1:g.33904C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.3397C=	ENSP00000338213.6:p.Pro1133=
ENST00000380518.8:c.3604C= MANE Select	ENSP00000369889.3:p.Pro1202=
ENST00000337299.6:c.3397C=	ENSP00000338213.6:p.Pro1133=
ENST00000380518.7:c.3604C=	ENSP00000369889.3:p.Pro1202=
ENST00000493991.5:n.2690C=
ENST00000546974.1:n.457C=
NM_001844.4:c.3604C=	NP_001835.3:p.Pro1202=
NM_033150.2:c.3397C=	NP_149162.2:p.Pro1133=
XM_006719242.2:c.3748C=	XP_006719305.2:p.Pro1250=
XM_011537928.1:c.3748C=	XP_011536230.1:p.Pro1250=
XM_011537929.1:c.3748C=	XP_011536231.1:p.Pro1250=
XM_011537930.1:c.3748C=	XP_011536232.1:p.Pro1250=
XM_011537931.1:c.3748C=	XP_011536233.1:p.Pro1250=
XM_011537932.1:c.3748C=	XP_011536234.1:p.Pro1250=
XM_011537933.1:c.3748C=	XP_011536235.1:p.Pro1250=
XM_011537934.1:c.3745C=	XP_011536236.1:p.Pro1249=
XM_011537935.1:c.2692C=	XP_011536237.1:p.Pro898=
XM_017018828.1:c.3748C=	XP_016874317.1:p.Pro1250=
XM_017018829.1:c.3745C=	XP_016874318.1:p.Pro1249=
XM_017018830.1:c.3538C=	XP_016874319.1:p.Pro1180=
XM_017018831.2:c.3058C=	XP_016874320.1:p.Pro1020=
NM_001844.5:c.3604C= MANE Select	NP_001835.3:p.Pro1202=
NM_033150.3:c.3397C=	NP_149162.2:p.Pro1133=