Canonical Allele Identifier: CA2653722060

Gene: COL9A3

Linked Data

• gnomAD v4: 20-62832283-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.62832283T>A , CM000682.2:g.62832283T>A	GRCh38
NC_000020.10:g.61463635T>A , CM000682.1:g.61463635T>A	GRCh37
NC_000020.9:g.60934080T>A	NCBI36
NG_016353.1:g.20222T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649368.1:c.1323+94T>A MANE Select	ENSP00000496793.1:n.1323+94T>A
ENST00000343916.7:c.1323+94T>A	ENSP00000341640.3:n.1323+94T>A
ENST00000466192.5:n.1050+94T>A
ENST00000469852.5:n.619+94T>A
ENST00000481800.1:n.296+94T>A
ENST00000490398.5:n.120+94T>A
NM_001853.3:c.1323+94T>A	NP_001844.3:n.1323+94T>A
XM_011528543.1:c.1323+94T>A	XP_011526845.1:n.1323+94T>A
XM_011528544.1:c.1116+94T>A	XP_011526846.1:n.1116+94T>A
XM_011528545.1:c.1323+94T>A	XP_011526847.1:n.1323+94T>A
XM_011528546.1:c.1323+94T>A	XP_011526848.1:n.1323+94T>A
XM_011528547.1:c.1323+94T>A	XP_011526849.1:n.1323+94T>A
XR_936499.1:n.1324+94T>A
NM_001853.4:c.1323+94T>A MANE Select	NP_001844.3:n.1323+94T>A
XM_017027666.1:c.1323+94T>A	XP_016883155.1:n.1323+94T>A