Canonical Allele Identifier: CA2034456272

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47985957G= , CM000674.2:g.47985957G=	GRCh38
NC_000012.11:g.48379740G= , CM000674.1:g.48379740G=	GRCh37
NC_000012.10:g.46666007G=	NCBI36
NG_008072.1:g.23546C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000337299.7:c.1329C=	ENSP00000338213.6:p.Pro443=
ENST00000380518.8:c.1536C= MANE Select	ENSP00000369889.3:p.Pro512=
ENST00000337299.6:c.1329C=	ENSP00000338213.6:p.Pro443=
ENST00000380518.7:c.1536C=	ENSP00000369889.3:p.Pro512=
ENST00000493991.5:n.460C=
NM_001844.4:c.1536C=	NP_001835.3:p.Pro512=
NM_033150.2:c.1329C=	NP_149162.2:p.Pro443=
XM_006719242.2:c.1680C=	XP_006719305.2:p.Pro560=
XM_011537928.1:c.1680C=	XP_011536230.1:p.Pro560=
XM_011537929.1:c.1680C=	XP_011536231.1:p.Pro560=
XM_011537930.1:c.1680C=	XP_011536232.1:p.Pro560=
XM_011537931.1:c.1680C=	XP_011536233.1:p.Pro560=
XM_011537932.1:c.1680C=	XP_011536234.1:p.Pro560=
XM_011537933.1:c.1680C=	XP_011536235.1:p.Pro560=
XM_011537934.1:c.1677C=	XP_011536236.1:p.Pro559=
XM_011537935.1:c.624C=	XP_011536237.1:p.Pro208=
XM_017018828.1:c.1680C=	XP_016874317.1:p.Pro560=
XM_017018829.1:c.1677C=	XP_016874318.1:p.Pro559=
XM_017018830.1:c.1470C=	XP_016874319.1:p.Pro490=
XM_017018831.2:c.990C=	XP_016874320.1:p.Pro330=
NM_001844.5:c.1536C= MANE Select	NP_001835.3:p.Pro512=
NM_033150.3:c.1329C=	NP_149162.2:p.Pro443=