Canonical Allele Identifier: CA9948984
Gene: COL9A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.62817090C>T , CM000682.2:g.62817090C>T GRCh38
NC_000020.10:g.61448442C>T , CM000682.1:g.61448442C>T GRCh37
NC_000020.9:g.60918887C>T NCBI36
NG_016353.1:g.5029C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000649368.1:c.26C>T MANE Select ENSP00000496793.1:p.Pro9Leu
ENST00000343916.7:c.26C>T ENSP00000341640.3:p.Pro9Leu
ENST00000477612.5:n.75-477C>T
NM_001853.3:c.26C>T NP_001844.3:p.Pro9Leu
XM_011528543.1:c.26C>T XP_011526845.1:p.Pro9Leu
XM_011528545.1:c.26C>T XP_011526847.1:p.Pro9Leu
XM_011528546.1:c.26C>T XP_011526848.1:p.Pro9Leu
XM_011528547.1:c.26C>T XP_011526849.1:p.Pro9Leu
XR_936499.1:n.27C>T
NM_001853.4:c.26C>T MANE Select NP_001844.3:p.Pro9Leu
XM_017027666.1:c.26C>T XP_016883155.1:p.Pro9Leu