Canonical Allele Identifier: CA2795861022

Gene: COL2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47973035A>C , CM000674.2:g.47973035A>C	GRCh38
NC_000012.11:g.48366818A>C , CM000674.1:g.48366818A>C	GRCh37
NC_000012.10:g.46653085A>C	NCBI36
NG_008072.1:g.36468T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380518.8:c.*372T>G MANE Select	ENSP00000369889.3:n.*372T>G
ENST00000380518.7:c.*372T>G	ENSP00000369889.3:n.*372T>G
NM_001844.4:c.*372T>G	NP_001835.3:n.*372T>G
NM_033150.2:c.*372T>G	NP_149162.2:n.*372T>G
XM_006719242.2:c.*372T>G	XP_006719305.2:n.*372T>G
XM_011537928.1:c.*372T>G	XP_011536230.1:n.*372T>G
XM_011537929.1:c.*372T>G	XP_011536231.1:n.*372T>G
XM_011537930.1:c.*372T>G	XP_011536232.1:n.*372T>G
XM_011537931.1:c.*372T>G	XP_011536233.1:n.*372T>G
XM_011537932.1:c.*372T>G	XP_011536234.1:n.*372T>G
XM_011537933.1:c.*372T>G	XP_011536235.1:n.*372T>G
XM_011537934.1:c.*372T>G	XP_011536236.1:n.*372T>G
XM_011537935.1:c.*372T>G	XP_011536237.1:n.*372T>G
XM_017018828.1:c.*372T>G	XP_016874317.1:n.*372T>G
XM_017018829.1:c.*372T>G	XP_016874318.1:n.*372T>G
XM_017018830.1:c.*372T>G	XP_016874319.1:n.*372T>G
XM_017018831.2:c.*372T>G	XP_016874320.1:n.*372T>G
NM_001844.5:c.*372T>G MANE Select	NP_001835.3:n.*372T>G
NM_033150.3:c.*372T>G	NP_149162.2:n.*372T>G