Canonical Allele Identifier: CA2374469790

Gene: COL9A3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.62832121_62832122delinsTC , CM000682.2:g.62832121_62832122delinsTC	GRCh38
NC_000020.10:g.61463473_61463474delinsTC , CM000682.1:g.61463473_61463474delinsTC	GRCh37
NC_000020.9:g.60933918_60933919delinsTC	NCBI36
NG_016353.1:g.20060_20061delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649368.1:c.1288-33_1288-32delinsTC MANE Select	ENSP00000496793.1:n.1288-33_1288-32delinsTC
ENST00000343916.7:c.1288-33_1288-32delinsTC	ENSP00000341640.3:n.1288-33_1288-32delinsTC
ENST00000466192.5:n.982_983delinsTC
ENST00000469852.5:n.551_552delinsTC
ENST00000481800.1:n.261-33_261-32delinsTC
ENST00000490398.5:n.85-33_85-32delinsTC
NM_001853.3:c.1288-33_1288-32delinsTC	NP_001844.3:n.1288-33_1288-32delinsTC
XM_011528543.1:c.1288-33_1288-32delinsTC	XP_011526845.1:n.1288-33_1288-32delinsTC
XM_011528544.1:c.1081-33_1081-32delinsTC	XP_011526846.1:n.1081-33_1081-32delinsTC
XM_011528545.1:c.1288-33_1288-32delinsTC	XP_011526847.1:n.1288-33_1288-32delinsTC
XM_011528546.1:c.1288-33_1288-32delinsTC	XP_011526848.1:n.1288-33_1288-32delinsTC
XM_011528547.1:c.1288-33_1288-32delinsTC	XP_011526849.1:n.1288-33_1288-32delinsTC
XR_936499.1:n.1289-33_1289-32delinsTC
NM_001853.4:c.1288-33_1288-32delinsTC MANE Select	NP_001844.3:n.1288-33_1288-32delinsTC
XM_017027666.1:c.1288-33_1288-32delinsTC	XP_016883155.1:n.1288-33_1288-32delinsTC