Canonical Allele Identifier: CA384536902

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48369297T>A (hg19) ; chr12:g.47975514T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47975514T>A , CM000674.2:g.47975514T>A	GRCh38
NC_000012.11:g.48369297T>A , CM000674.1:g.48369297T>A	GRCh37
NC_000012.10:g.46655564T>A	NCBI36
NG_008072.1:g.33989A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.3482A>T	ENSP00000338213.6:p.Glu1161Val
ENST00000380518.8:c.3689A>T MANE Select	ENSP00000369889.3:p.Glu1230Val
ENST00000337299.6:c.3482A>T	ENSP00000338213.6:p.Glu1161Val
ENST00000380518.7:c.3689A>T	ENSP00000369889.3:p.Glu1230Val
ENST00000493991.5:n.2775A>T
ENST00000546974.1:n.542A>T
NM_001844.4:c.3689A>T	NP_001835.3:p.Glu1230Val
NM_033150.2:c.3482A>T	NP_149162.2:p.Glu1161Val
XM_006719242.2:c.3833A>T	XP_006719305.2:p.Glu1278Val
XM_011537928.1:c.3833A>T	XP_011536230.1:p.Glu1278Val
XM_011537929.1:c.3833A>T	XP_011536231.1:p.Glu1278Val
XM_011537930.1:c.3833A>T	XP_011536232.1:p.Glu1278Val
XM_011537931.1:c.3833A>T	XP_011536233.1:p.Glu1278Val
XM_011537932.1:c.3833A>T	XP_011536234.1:p.Glu1278Val
XM_011537933.1:c.3833A>T	XP_011536235.1:p.Glu1278Val
XM_011537934.1:c.3830A>T	XP_011536236.1:p.Glu1277Val
XM_011537935.1:c.2777A>T	XP_011536237.1:p.Glu926Val
XM_017018828.1:c.3833A>T	XP_016874317.1:p.Glu1278Val
XM_017018829.1:c.3830A>T	XP_016874318.1:p.Glu1277Val
XM_017018830.1:c.3623A>T	XP_016874319.1:p.Glu1208Val
XM_017018831.2:c.3143A>T	XP_016874320.1:p.Glu1048Val
NM_001844.5:c.3689A>T MANE Select	NP_001835.3:p.Glu1230Val
NM_033150.3:c.3482A>T	NP_149162.2:p.Glu1161Val