Canonical Allele Identifier: CA2034449175

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47982142C= , CM000674.2:g.47982142C=	GRCh38
NC_000012.11:g.48375925C= , CM000674.1:g.48375925C=	GRCh37
NC_000012.10:g.46662192C=	NCBI36
NG_008072.1:g.27361G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001844.5:c.2320G= MANE Select	NP_001835.3:p.Gly774=
ENST00000380518.8:c.2320G= MANE Select	ENSP00000369889.3:p.Gly774=
NM_001844.4:c.2320G=	NP_001835.3:p.Gly774=
NM_033150.2:c.2113G=	NP_149162.2:p.Gly705=
NM_033150.3:c.2113G=	NP_149162.2:p.Gly705=
ENST00000337299.6:c.2113G=	ENSP00000338213.6:p.Gly705=
ENST00000337299.7:c.2113G=	ENSP00000338213.6:p.Gly705=
ENST00000380518.7:c.2320G=	ENSP00000369889.3:p.Gly774=
ENST00000483376.1:n.498G=
ENST00000493991.5:n.1244G=
XM_006719242.2:c.2464G=	XP_006719305.2:p.Gly822=
XM_011537928.1:c.2464G=	XP_011536230.1:p.Gly822=
XM_011537929.1:c.2464G=	XP_011536231.1:p.Gly822=
XM_011537930.1:c.2464G=	XP_011536232.1:p.Gly822=
XM_011537931.1:c.2464G=	XP_011536233.1:p.Gly822=
XM_011537932.1:c.2464G=	XP_011536234.1:p.Gly822=
XM_011537933.1:c.2464G=	XP_011536235.1:p.Gly822=
XM_011537934.1:c.2461G=	XP_011536236.1:p.Gly821=
XM_011537935.1:c.1408G=	XP_011536237.1:p.Gly470=
XM_017018828.1:c.2464G=	XP_016874317.1:p.Gly822=
XM_017018829.1:c.2461G=	XP_016874318.1:p.Gly821=
XM_017018830.1:c.2254G=	XP_016874319.1:p.Gly752=
XM_017018831.2:c.1774G=	XP_016874320.1:p.Gly592=
XR_944910.1:n.209-273C=