Canonical Allele Identifier: CA2374469770
Gene: COL9A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62832077C= , CM000682.2:g.62832077C= GRCh38
NC_000020.10:g.61463429C= , CM000682.1:g.61463429C= GRCh37
NC_000020.9:g.60933874C= NCBI36
NG_016353.1:g.20016C=

Transcript Alleles

HGVS Amino-acid change
ENST00000649368.1:c.1288-77C= MANE Select ENSP00000496793.1:n.1288-77C=
ENST00000343916.7:c.1288-77C= ENSP00000341640.3:n.1288-77C=
ENST00000466192.5:n.938C=
ENST00000469852.5:n.507C=
ENST00000481800.1:n.261-77C=
ENST00000490398.5:n.85-77C=
NM_001853.3:c.1288-77C= NP_001844.3:n.1288-77C=
XM_011528543.1:c.1288-77C= XP_011526845.1:n.1288-77C=
XM_011528544.1:c.1081-77C= XP_011526846.1:n.1081-77C=
XM_011528545.1:c.1288-77C= XP_011526847.1:n.1288-77C=
XM_011528546.1:c.1288-77C= XP_011526848.1:n.1288-77C=
XM_011528547.1:c.1288-77C= XP_011526849.1:n.1288-77C=
XR_936499.1:n.1289-77C=
NM_001853.4:c.1288-77C= MANE Select NP_001844.3:n.1288-77C=
XM_017027666.1:c.1288-77C= XP_016883155.1:n.1288-77C=