Canonical Allele Identifier: CA479442090

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48389679A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47995896A>C , CM000674.2:g.47995896A>C	GRCh38
NC_000012.11:g.48389679A>C , CM000674.1:g.48389679A>C	GRCh37
NC_000012.10:g.46675946A>C	NCBI36
NG_008072.1:g.13607T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000337299.7:c.426T>G	ENSP00000338213.6:p.Pro142=
ENST00000380518.8:c.633T>G MANE Select	ENSP00000369889.3:p.Pro211=
ENST00000337299.6:c.426T>G	ENSP00000338213.6:p.Pro142=
ENST00000380518.7:c.633T>G	ENSP00000369889.3:p.Pro211=
NM_001844.4:c.633T>G	NP_001835.3:p.Pro211=
NM_033150.2:c.426T>G	NP_149162.2:p.Pro142=
XM_006719242.2:c.777T>G	XP_006719305.2:p.Pro259=
XM_011537928.1:c.777T>G	XP_011536230.1:p.Pro259=
XM_011537929.1:c.777T>G	XP_011536231.1:p.Pro259=
XM_011537930.1:c.777T>G	XP_011536232.1:p.Pro259=
XM_011537931.1:c.777T>G	XP_011536233.1:p.Pro259=
XM_011537932.1:c.777T>G	XP_011536234.1:p.Pro259=
XM_011537933.1:c.777T>G	XP_011536235.1:p.Pro259=
XM_011537934.1:c.774T>G	XP_011536236.1:p.Pro258=
XM_017018828.1:c.777T>G	XP_016874317.1:p.Pro259=
XM_017018829.1:c.774T>G	XP_016874318.1:p.Pro258=
XM_017018830.1:c.567T>G	XP_016874319.1:p.Pro189=
XM_017018831.2:c.87T>G	XP_016874320.1:p.Pro29=
NM_001844.5:c.633T>G MANE Select	NP_001835.3:p.Pro211=
NM_033150.3:c.426T>G	NP_149162.2:p.Pro142=