Canonical Allele Identifier: CA2577447887
Gene: COL9A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62817596_62817604del , CM000682.2:g.62817596_62817604del GRCh38
NC_000020.10:g.61448948_61448956del , CM000682.1:g.61448948_61448956del GRCh37
NC_000020.9:g.60919393_60919401del NCBI36
NG_016353.1:g.5535_5543del

Transcript Alleles

HGVS Amino-acid Change
ENST00000649368.1:c.108_116del MANE Select ENSP00000496793.1:p.Pro37_Pro39del
ENST00000343916.7:c.108_116del ENSP00000341640.3:p.Pro37_Pro39del
ENST00000477612.5:n.104_112del
ENST00000489045.5:n.154_162del
NM_001853.3:c.108_116del NP_001844.3:p.Pro37_Pro39del
XM_011528543.1:c.108_116del XP_011526845.1:p.Pro37_Pro39del
XM_011528545.1:c.108_116del XP_011526847.1:p.Pro37_Pro39del
XM_011528546.1:c.108_116del XP_011526848.1:p.Pro37_Pro39del
XM_011528547.1:c.108_116del XP_011526849.1:p.Pro37_Pro39del
XR_936499.1:n.109_117del
NM_001853.4:c.108_116del MANE Select NP_001844.3:p.Pro37_Pro39del
XM_017027666.1:c.108_116del XP_016883155.1:p.Pro37_Pro39del