Canonical Allele Identifier: CA384525984

Gene: COL2A1

Linked Data

• ClinVar Variation Id: 2069856
• ClinVar RCV Id: RCV002958932
• MyVariant Identifiers: chr12:g.48393748G>T (hg19) ; chr12:g.47999965G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47999965G>T , CM000674.2:g.47999965G>T	GRCh38
NC_000012.11:g.48393748G>T , CM000674.1:g.48393748G>T	GRCh37
NC_000012.10:g.46680015G>T	NCBI36
NG_008072.1:g.9538C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000337299.7:c.86-1534C>A	ENSP00000338213.6:n.86-1534C>A
ENST00000380518.8:c.246C>A MANE Select	ENSP00000369889.3:p.Phe82Leu
ENST00000490609.2:n.479C>A
ENST00000337299.6:c.86-1534C>A	ENSP00000338213.6:n.86-1534C>A
ENST00000380518.7:c.246C>A	ENSP00000369889.3:p.Phe82Leu
ENST00000474996.6:n.484C>A
ENST00000490609.1:n.411C>A
NM_001844.4:c.246C>A	NP_001835.3:p.Phe82Leu
NM_033150.2:c.86-1534C>A	NP_149162.2:n.86-1534C>A
XM_006719242.2:c.387C>A	XP_006719305.2:p.Phe129Leu
XM_011537928.1:c.387C>A	XP_011536230.1:p.Phe129Leu
XM_011537929.1:c.387C>A	XP_011536231.1:p.Phe129Leu
XM_011537930.1:c.387C>A	XP_011536232.1:p.Phe129Leu
XM_011537931.1:c.387C>A	XP_011536233.1:p.Phe129Leu
XM_011537932.1:c.387C>A	XP_011536234.1:p.Phe129Leu
XM_011537933.1:c.387C>A	XP_011536235.1:p.Phe129Leu
XM_011537934.1:c.387C>A	XP_011536236.1:p.Phe129Leu
XM_017018828.1:c.387C>A	XP_016874317.1:p.Phe129Leu
XM_017018829.1:c.387C>A	XP_016874318.1:p.Phe129Leu
XM_017018830.1:c.227-1534C>A	XP_016874319.1:n.227-1534C>A
XM_017018831.2:c.-301C>A	XP_016874320.1:n.-301C>A
NM_001844.5:c.246C>A MANE Select	NP_001835.3:p.Phe82Leu
NM_033150.3:c.86-1534C>A	NP_149162.2:n.86-1534C>A