Canonical Allele Identifier: CA2374469822

Gene: COL9A3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.62832174C= , CM000682.2:g.62832174C=	GRCh38
NC_000020.10:g.61463526C= , CM000682.1:g.61463526C=	GRCh37
NC_000020.9:g.60933971C=	NCBI36
NG_016353.1:g.20113C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000649368.1:c.1308C= MANE Select	ENSP00000496793.1:p.Gly436=
ENST00000343916.7:c.1308C=	ENSP00000341640.3:p.Gly436=
ENST00000466192.5:n.1035C=
ENST00000469852.5:n.604C=
ENST00000481800.1:n.281C=
ENST00000490398.5:n.105C=
NM_001853.3:c.1308C=	NP_001844.3:p.Gly436=
XM_011528543.1:c.1308C=	XP_011526845.1:p.Gly436=
XM_011528544.1:c.1101C=	XP_011526846.1:p.Gly367=
XM_011528545.1:c.1308C=	XP_011526847.1:p.Gly436=
XM_011528546.1:c.1308C=	XP_011526848.1:p.Gly436=
XM_011528547.1:c.1308C=	XP_011526849.1:p.Gly436=
XR_936499.1:n.1309C=
NM_001853.4:c.1308C= MANE Select	NP_001844.3:p.Gly436=
XM_017027666.1:c.1308C=	XP_016883155.1:p.Gly436=