Canonical Allele Identifier: CA2034479685
Gene: COL2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47995893T= , CM000674.2:g.47995893T= GRCh38
NC_000012.11:g.48389676T= , CM000674.1:g.48389676T= GRCh37
NC_000012.10:g.46675943T= NCBI36
NG_008072.1:g.13610A=

Transcript Alleles

HGVS Amino-acid change
ENST00000337299.7:c.429A= ENSP00000338213.6:p.Pro143=
ENST00000380518.8:c.636A= MANE Select ENSP00000369889.3:p.Pro212=
ENST00000337299.6:c.429A= ENSP00000338213.6:p.Pro143=
ENST00000380518.7:c.636A= ENSP00000369889.3:p.Pro212=
NM_001844.4:c.636A= NP_001835.3:p.Pro212=
NM_033150.2:c.429A= NP_149162.2:p.Pro143=
XM_006719242.2:c.780A= XP_006719305.2:p.Pro260=
XM_011537928.1:c.780A= XP_011536230.1:p.Pro260=
XM_011537929.1:c.780A= XP_011536231.1:p.Pro260=
XM_011537930.1:c.780A= XP_011536232.1:p.Pro260=
XM_011537931.1:c.780A= XP_011536233.1:p.Pro260=
XM_011537932.1:c.780A= XP_011536234.1:p.Pro260=
XM_011537933.1:c.780A= XP_011536235.1:p.Pro260=
XM_011537934.1:c.777A= XP_011536236.1:p.Pro259=
XM_017018828.1:c.780A= XP_016874317.1:p.Pro260=
XM_017018829.1:c.777A= XP_016874318.1:p.Pro259=
XM_017018830.1:c.570A= XP_016874319.1:p.Pro190=
XM_017018831.2:c.90A= XP_016874320.1:p.Pro30=
NM_001844.5:c.636A= MANE Select NP_001835.3:p.Pro212=
NM_033150.3:c.429A= NP_149162.2:p.Pro143=