Canonical Allele Identifier: CA479442096

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48389685T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47995902T>A , CM000674.2:g.47995902T>A	GRCh38
NC_000012.11:g.48389685T>A , CM000674.1:g.48389685T>A	GRCh37
NC_000012.10:g.46675952T>A	NCBI36
NG_008072.1:g.13601A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.420A>T	ENSP00000338213.6:p.Arg140=
ENST00000380518.8:c.627A>T MANE Select	ENSP00000369889.3:p.Arg209=
ENST00000337299.6:c.420A>T	ENSP00000338213.6:p.Arg140=
ENST00000380518.7:c.627A>T	ENSP00000369889.3:p.Arg209=
NM_001844.4:c.627A>T	NP_001835.3:p.Arg209=
NM_033150.2:c.420A>T	NP_149162.2:p.Arg140=
XM_006719242.2:c.771A>T	XP_006719305.2:p.Arg257=
XM_011537928.1:c.771A>T	XP_011536230.1:p.Arg257=
XM_011537929.1:c.771A>T	XP_011536231.1:p.Arg257=
XM_011537930.1:c.771A>T	XP_011536232.1:p.Arg257=
XM_011537931.1:c.771A>T	XP_011536233.1:p.Arg257=
XM_011537932.1:c.771A>T	XP_011536234.1:p.Arg257=
XM_011537933.1:c.771A>T	XP_011536235.1:p.Arg257=
XM_011537934.1:c.768A>T	XP_011536236.1:p.Arg256=
XM_017018828.1:c.771A>T	XP_016874317.1:p.Arg257=
XM_017018829.1:c.768A>T	XP_016874318.1:p.Arg256=
XM_017018830.1:c.561A>T	XP_016874319.1:p.Arg187=
XM_017018831.2:c.81A>T	XP_016874320.1:p.Arg27=
NM_001844.5:c.627A>T MANE Select	NP_001835.3:p.Arg209=
NM_033150.3:c.420A>T	NP_149162.2:p.Arg140=