Canonical Allele Identifier: CA2374469814

Gene: COL9A3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.62832159G= , CM000682.2:g.62832159G=	GRCh38
NC_000020.10:g.61463511G= , CM000682.1:g.61463511G=	GRCh37
NC_000020.9:g.60933956G=	NCBI36
NG_016353.1:g.20098G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649368.1:c.1293G= MANE Select	ENSP00000496793.1:p.Pro431=
ENST00000343916.7:c.1293G=	ENSP00000341640.3:p.Pro431=
ENST00000466192.5:n.1020G=
ENST00000469852.5:n.589G=
ENST00000481800.1:n.266G=
ENST00000490398.5:n.90G=
NM_001853.3:c.1293G=	NP_001844.3:p.Pro431=
XM_011528543.1:c.1293G=	XP_011526845.1:p.Pro431=
XM_011528544.1:c.1086G=	XP_011526846.1:p.Pro362=
XM_011528545.1:c.1293G=	XP_011526847.1:p.Pro431=
XM_011528546.1:c.1293G=	XP_011526848.1:p.Pro431=
XM_011528547.1:c.1293G=	XP_011526849.1:p.Pro431=
XR_936499.1:n.1294G=
NM_001853.4:c.1293G= MANE Select	NP_001844.3:p.Pro431=
XM_017027666.1:c.1293G=	XP_016883155.1:p.Pro431=