Canonical Allele Identifier: CA2374469776

Gene: COL9A3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.62832091G= , CM000682.2:g.62832091G=	GRCh38
NC_000020.10:g.61463443G= , CM000682.1:g.61463443G=	GRCh37
NC_000020.9:g.60933888G=	NCBI36
NG_016353.1:g.20030G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649368.1:c.1288-63G= MANE Select	ENSP00000496793.1:n.1288-63G=
ENST00000343916.7:c.1288-63G=	ENSP00000341640.3:n.1288-63G=
ENST00000466192.5:n.952G=
ENST00000469852.5:n.521G=
ENST00000481800.1:n.261-63G=
ENST00000490398.5:n.85-63G=
NM_001853.3:c.1288-63G=	NP_001844.3:n.1288-63G=
XM_011528543.1:c.1288-63G=	XP_011526845.1:n.1288-63G=
XM_011528544.1:c.1081-63G=	XP_011526846.1:n.1081-63G=
XM_011528545.1:c.1288-63G=	XP_011526847.1:n.1288-63G=
XM_011528546.1:c.1288-63G=	XP_011526848.1:n.1288-63G=
XM_011528547.1:c.1288-63G=	XP_011526849.1:n.1288-63G=
XR_936499.1:n.1289-63G=
NM_001853.4:c.1288-63G= MANE Select	NP_001844.3:n.1288-63G=
XM_017027666.1:c.1288-63G=	XP_016883155.1:n.1288-63G=