Canonical Allele Identifier: CA479454313

Gene: COL2A1

Linked Data

• MyVariant Identifiers: chr12:g.48371413G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47977630G>A , CM000674.2:g.47977630G>A	GRCh38
NC_000012.11:g.48371413G>A , CM000674.1:g.48371413G>A	GRCh37
NC_000012.10:g.46657680G>A	NCBI36
NG_008072.1:g.31873C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.2928C>T	ENSP00000338213.6:p.Pro976=
ENST00000380518.8:c.3135C>T MANE Select	ENSP00000369889.3:p.Pro1045=
ENST00000337299.6:c.2928C>T	ENSP00000338213.6:p.Pro976=
ENST00000380518.7:c.3135C>T	ENSP00000369889.3:p.Pro1045=
ENST00000493991.5:n.2221C>T
NM_001844.4:c.3135C>T	NP_001835.3:p.Pro1045=
NM_033150.2:c.2928C>T	NP_149162.2:p.Pro976=
XM_006719242.2:c.3279C>T	XP_006719305.2:p.Pro1093=
XM_011537928.1:c.3279C>T	XP_011536230.1:p.Pro1093=
XM_011537929.1:c.3279C>T	XP_011536231.1:p.Pro1093=
XM_011537930.1:c.3279C>T	XP_011536232.1:p.Pro1093=
XM_011537931.1:c.3279C>T	XP_011536233.1:p.Pro1093=
XM_011537932.1:c.3279C>T	XP_011536234.1:p.Pro1093=
XM_011537933.1:c.3279C>T	XP_011536235.1:p.Pro1093=
XM_011537934.1:c.3276C>T	XP_011536236.1:p.Pro1092=
XM_011537935.1:c.2223C>T	XP_011536237.1:p.Pro741=
XM_017018828.1:c.3279C>T	XP_016874317.1:p.Pro1093=
XM_017018829.1:c.3276C>T	XP_016874318.1:p.Pro1092=
XM_017018830.1:c.3069C>T	XP_016874319.1:p.Pro1023=
XM_017018831.2:c.2589C>T	XP_016874320.1:p.Pro863=
NM_001844.5:c.3135C>T MANE Select	NP_001835.3:p.Pro1045=
NM_033150.3:c.2928C>T	NP_149162.2:p.Pro976=