Canonical Allele Identifier: CA2034475966
Gene: COL2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47976862G= , CM000674.2:g.47976862G= GRCh38
NC_000012.11:g.48370645G= , CM000674.1:g.48370645G= GRCh37
NC_000012.10:g.46656912G= NCBI36
NG_008072.1:g.32641C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337299.7:c.3178C= ENSP00000338213.6:p.Leu1060=
ENST00000380518.8:c.3385C= MANE Select ENSP00000369889.3:p.Leu1129=
ENST00000337299.6:c.3178C= ENSP00000338213.6:p.Leu1060=
ENST00000380518.7:c.3385C= ENSP00000369889.3:p.Leu1129=
ENST00000493991.5:n.2471C=
ENST00000546974.1:n.238C=
NM_001844.4:c.3385C= NP_001835.3:p.Leu1129=
NM_033150.2:c.3178C= NP_149162.2:p.Leu1060=
XM_006719242.2:c.3529C= XP_006719305.2:p.Leu1177=
XM_011537928.1:c.3529C= XP_011536230.1:p.Leu1177=
XM_011537929.1:c.3529C= XP_011536231.1:p.Leu1177=
XM_011537930.1:c.3529C= XP_011536232.1:p.Leu1177=
XM_011537931.1:c.3529C= XP_011536233.1:p.Leu1177=
XM_011537932.1:c.3529C= XP_011536234.1:p.Leu1177=
XM_011537933.1:c.3529C= XP_011536235.1:p.Leu1177=
XM_011537934.1:c.3526C= XP_011536236.1:p.Leu1176=
XM_011537935.1:c.2473C= XP_011536237.1:p.Leu825=
XM_017018828.1:c.3529C= XP_016874317.1:p.Leu1177=
XM_017018829.1:c.3526C= XP_016874318.1:p.Leu1176=
XM_017018830.1:c.3319C= XP_016874319.1:p.Leu1107=
XM_017018831.2:c.2839C= XP_016874320.1:p.Leu947=
NM_001844.5:c.3385C= MANE Select NP_001835.3:p.Leu1129=
NM_033150.3:c.3178C= NP_149162.2:p.Leu1060=