Canonical Allele Identifier: CA2034489362

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48000096G= , CM000674.2:g.48000096G=	GRCh38
NC_000012.11:g.48393879G= , CM000674.1:g.48393879G=	GRCh37
NC_000012.10:g.46680146G=	NCBI36
NG_008072.1:g.9407C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.86-1665C=	ENSP00000338213.6:n.86-1665C=
ENST00000380518.8:c.115C= MANE Select	ENSP00000369889.3:p.Gln39=
ENST00000490609.2:n.348C=
ENST00000337299.6:c.86-1665C=	ENSP00000338213.6:n.86-1665C=
ENST00000380518.7:c.115C=	ENSP00000369889.3:p.Gln39=
ENST00000474996.6:n.353C=
ENST00000490609.1:n.280C=
NM_001844.4:c.115C=	NP_001835.3:p.Gln39=
NM_033150.2:c.86-1665C=	NP_149162.2:n.86-1665C=
XM_006719242.2:c.256C=	XP_006719305.2:p.Gln86=
XM_011537928.1:c.256C=	XP_011536230.1:p.Gln86=
XM_011537929.1:c.256C=	XP_011536231.1:p.Gln86=
XM_011537930.1:c.256C=	XP_011536232.1:p.Gln86=
XM_011537931.1:c.256C=	XP_011536233.1:p.Gln86=
XM_011537932.1:c.256C=	XP_011536234.1:p.Gln86=
XM_011537933.1:c.256C=	XP_011536235.1:p.Gln86=
XM_011537934.1:c.256C=	XP_011536236.1:p.Gln86=
XM_017018828.1:c.256C=	XP_016874317.1:p.Gln86=
XM_017018829.1:c.256C=	XP_016874318.1:p.Gln86=
XM_017018830.1:c.227-1665C=	XP_016874319.1:n.227-1665C=
XM_017018831.2:c.-432C=	XP_016874320.1:n.-432C=
NM_001844.5:c.115C= MANE Select	NP_001835.3:p.Gln39=
NM_033150.3:c.86-1665C=	NP_149162.2:n.86-1665C=