Canonical Allele Identifier: CA2374462519

Gene: COL9A3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.62819980C= , CM000682.2:g.62819980C=	GRCh38
NC_000020.10:g.61451332C= , CM000682.1:g.61451332C=	GRCh37
NC_000020.9:g.60921777C=	NCBI36
NG_016353.1:g.7919C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001853.4:c.307C= MANE Select	NP_001844.3:p.Arg103=
ENST00000649368.1:c.307C= MANE Select	ENSP00000496793.1:p.Arg103=
NM_001853.3:c.307C=	NP_001844.3:p.Arg103=
ENST00000343916.7:c.307C=	ENSP00000341640.3:p.Arg103=
ENST00000452372.1:c.196C=	ENSP00000394280.1:p.Arg66=
ENST00000452372.2:c.196C=	ENSP00000394280.1:p.Arg66=
ENST00000477612.5:n.303C=
ENST00000489045.5:n.353C=
XM_011528543.1:c.307C=	XP_011526845.1:p.Arg103=
XM_011528544.1:c.36C=	XP_011526846.1:p.Asn12=
XM_011528545.1:c.307C=	XP_011526847.1:p.Arg103=
XM_011528546.1:c.307C=	XP_011526848.1:p.Arg103=
XM_011528547.1:c.307C=	XP_011526849.1:p.Arg103=
XM_017027666.1:c.307C=	XP_016883155.1:p.Arg103=
XR_936499.1:n.308C=