Canonical Allele Identifier: CA409587102
Community Standard Title: NM_001853.4(COL9A3):c.101C>G (p.Pro34Arg)
Gene: COL9A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62817589C>G , CM000682.2:g.62817589C>G GRCh38
NC_000020.10:g.61448941C>G , CM000682.1:g.61448941C>G GRCh37
NC_000020.9:g.60919386C>G NCBI36
NG_016353.1:g.5528C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001853.4:c.101C>G MANE Select NP_001844.3:p.Pro34Arg
ENST00000649368.1:c.101C>G MANE Select ENSP00000496793.1:p.Pro34Arg
NM_001853.3:c.101C>G NP_001844.3:p.Pro34Arg
ENST00000343916.7:c.101C>G ENSP00000341640.3:p.Pro34Arg
ENST00000477612.5:n.97C>G
ENST00000489045.5:n.147C>G
XM_011528543.1:c.101C>G XP_011526845.1:p.Pro34Arg
XM_011528545.1:c.101C>G XP_011526847.1:p.Pro34Arg
XM_011528546.1:c.101C>G XP_011526848.1:p.Pro34Arg
XM_011528547.1:c.101C>G XP_011526849.1:p.Pro34Arg
XM_017027666.1:c.101C>G XP_016883155.1:p.Pro34Arg
XR_936499.1:n.102C>G