Canonical Allele Identifier: CA2374469745
Gene: COL9A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62832025G= , CM000682.2:g.62832025G= GRCh38
NC_000020.10:g.61463377G= , CM000682.1:g.61463377G= GRCh37
NC_000020.9:g.60933822G= NCBI36
NG_016353.1:g.19964G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649368.1:c.1288-129G= MANE Select ENSP00000496793.1:n.1288-129G=
ENST00000343916.7:c.1288-129G= ENSP00000341640.3:n.1288-129G=
ENST00000466192.5:n.886G=
ENST00000469852.5:n.455G=
ENST00000481800.1:n.260+38G=
ENST00000490398.5:n.85-129G=
NM_001853.3:c.1288-129G= NP_001844.3:n.1288-129G=
XM_011528543.1:c.1288-129G= XP_011526845.1:n.1288-129G=
XM_011528544.1:c.1081-129G= XP_011526846.1:n.1081-129G=
XM_011528545.1:c.1288-129G= XP_011526847.1:n.1288-129G=
XM_011528546.1:c.1288-129G= XP_011526848.1:n.1288-129G=
XM_011528547.1:c.1288-129G= XP_011526849.1:n.1288-129G=
XR_936499.1:n.1289-129G=
NM_001853.4:c.1288-129G= MANE Select NP_001844.3:n.1288-129G=
XM_017027666.1:c.1288-129G= XP_016883155.1:n.1288-129G=