Canonical Allele Identifier: CA384523847
Gene: COL2A1 HGNC NCBI

Linked Data

dbSNP Id: rs1232544067

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.47995880C>T , CM000674.2:g.47995880C>T GRCh38
NC_000012.11:g.48389663C>T , CM000674.1:g.48389663C>T GRCh37
NC_000012.10:g.46675930C>T NCBI36
NG_008072.1:g.13623G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000337299.7:c.442G>A ENSP00000338213.6:p.Ala148Thr
ENST00000380518.8:c.649G>A MANE Select ENSP00000369889.3:p.Ala217Thr
ENST00000337299.6:c.442G>A ENSP00000338213.6:p.Ala148Thr
ENST00000380518.7:c.649G>A ENSP00000369889.3:p.Ala217Thr
NM_001844.4:c.649G>A NP_001835.3:p.Ala217Thr
NM_033150.2:c.442G>A NP_149162.2:p.Ala148Thr
XM_006719242.2:c.793G>A XP_006719305.2:p.Ala265Thr
XM_011537928.1:c.793G>A XP_011536230.1:p.Ala265Thr
XM_011537929.1:c.793G>A XP_011536231.1:p.Ala265Thr
XM_011537930.1:c.793G>A XP_011536232.1:p.Ala265Thr
XM_011537931.1:c.793G>A XP_011536233.1:p.Ala265Thr
XM_011537932.1:c.793G>A XP_011536234.1:p.Ala265Thr
XM_011537933.1:c.793G>A XP_011536235.1:p.Ala265Thr
XM_011537934.1:c.790G>A XP_011536236.1:p.Ala264Thr
XM_017018828.1:c.793G>A XP_016874317.1:p.Ala265Thr
XM_017018829.1:c.790G>A XP_016874318.1:p.Ala264Thr
XM_017018830.1:c.583G>A XP_016874319.1:p.Ala195Thr
XM_017018831.2:c.103G>A XP_016874320.1:p.Ala35Thr
NM_001844.5:c.649G>A MANE Select NP_001835.3:p.Ala217Thr
NM_033150.3:c.442G>A NP_149162.2:p.Ala148Thr