Canonical Allele Identifier: CA9949124
Community Standard Title: NM_001853.4(COL9A3):c.268C>T (p.Arg90Ter)
Gene: COL9A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62819941C>T , CM000682.2:g.62819941C>T GRCh38
NC_000020.10:g.61451293C>T , CM000682.1:g.61451293C>T GRCh37
NC_000020.9:g.60921738C>T NCBI36
NG_016353.1:g.7880C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001853.4:c.268C>T MANE Select NP_001844.3:p.Arg90Ter
ENST00000649368.1:c.268C>T MANE Select ENSP00000496793.1:p.Arg90Ter
NM_001853.3:c.268C>T NP_001844.3:p.Arg90Ter
ENST00000343916.7:c.268C>T ENSP00000341640.3:p.Arg90Ter
ENST00000452372.1:c.157C>T ENSP00000394280.1:p.Arg53Ter
ENST00000452372.2:c.157C>T ENSP00000394280.1:p.Arg53Ter
ENST00000477612.5:n.264C>T
ENST00000489045.5:n.314C>T
XM_011528543.1:c.268C>T XP_011526845.1:p.Arg90Ter
XM_011528544.1:c.-4C>T XP_011526846.1:n.-4C>T
XM_011528545.1:c.268C>T XP_011526847.1:p.Arg90Ter
XM_011528546.1:c.268C>T XP_011526848.1:p.Arg90Ter
XM_011528547.1:c.268C>T XP_011526849.1:p.Arg90Ter
XM_017027666.1:c.268C>T XP_016883155.1:p.Arg90Ter
XR_936499.1:n.269C>T