Canonical Allele Identifier: CA409587048
Gene: COL9A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62817573G>A , CM000682.2:g.62817573G>A GRCh38
NC_000020.10:g.61448925G>A , CM000682.1:g.61448925G>A GRCh37
NC_000020.9:g.60919370G>A NCBI36
NG_016353.1:g.5512G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000649368.1:c.85G>A MANE Select ENSP00000496793.1:p.Gly29Arg
ENST00000343916.7:c.85G>A ENSP00000341640.3:p.Gly29Arg
ENST00000477612.5:n.81G>A
ENST00000489045.5:n.131G>A
NM_001853.3:c.85G>A NP_001844.3:p.Gly29Arg
XM_011528543.1:c.85G>A XP_011526845.1:p.Gly29Arg
XM_011528545.1:c.85G>A XP_011526847.1:p.Gly29Arg
XM_011528546.1:c.85G>A XP_011526848.1:p.Gly29Arg
XM_011528547.1:c.85G>A XP_011526849.1:p.Gly29Arg
XR_936499.1:n.86G>A
NM_001853.4:c.85G>A MANE Select NP_001844.3:p.Gly29Arg
XM_017027666.1:c.85G>A XP_016883155.1:p.Gly29Arg