Canonical Allele Identifier: CA384523908

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48389681G>T (hg19) ; chr12:g.47995898G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47995898G>T , CM000674.2:g.47995898G>T	GRCh38
NC_000012.11:g.48389681G>T , CM000674.1:g.48389681G>T	GRCh37
NC_000012.10:g.46675948G>T	NCBI36
NG_008072.1:g.13605C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000337299.7:c.424C>A	ENSP00000338213.6:p.Pro142Thr
ENST00000380518.8:c.631C>A MANE Select	ENSP00000369889.3:p.Pro211Thr
ENST00000337299.6:c.424C>A	ENSP00000338213.6:p.Pro142Thr
ENST00000380518.7:c.631C>A	ENSP00000369889.3:p.Pro211Thr
NM_001844.4:c.631C>A	NP_001835.3:p.Pro211Thr
NM_033150.2:c.424C>A	NP_149162.2:p.Pro142Thr
XM_006719242.2:c.775C>A	XP_006719305.2:p.Pro259Thr
XM_011537928.1:c.775C>A	XP_011536230.1:p.Pro259Thr
XM_011537929.1:c.775C>A	XP_011536231.1:p.Pro259Thr
XM_011537930.1:c.775C>A	XP_011536232.1:p.Pro259Thr
XM_011537931.1:c.775C>A	XP_011536233.1:p.Pro259Thr
XM_011537932.1:c.775C>A	XP_011536234.1:p.Pro259Thr
XM_011537933.1:c.775C>A	XP_011536235.1:p.Pro259Thr
XM_011537934.1:c.772C>A	XP_011536236.1:p.Pro258Thr
XM_017018828.1:c.775C>A	XP_016874317.1:p.Pro259Thr
XM_017018829.1:c.772C>A	XP_016874318.1:p.Pro258Thr
XM_017018830.1:c.565C>A	XP_016874319.1:p.Pro189Thr
XM_017018831.2:c.85C>A	XP_016874320.1:p.Pro29Thr
NM_001844.5:c.631C>A MANE Select	NP_001835.3:p.Pro211Thr
NM_033150.3:c.424C>A	NP_149162.2:p.Pro142Thr