Canonical Allele Identifier: CA2006890362
Gene: CDON HGNC NCBI
VSIG10L2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.125956724A= , CM000673.2:g.125956724A= GRCh38
NC_000011.9:g.125826619A= , CM000673.1:g.125826619A= GRCh37
NC_000011.8:g.125331829A= NCBI36
NG_029776.1:g.111569T=

Transcript Alleles

HGVS Amino-acid change
ENST00000684078.1:c.*4218T= (CDON) ENSP00000507318.1:n.*4218T=
ENST00000638636.2:c.3114A= (VSIG10L2) ENSP00000491467.1:n.3114A=
ENST00000392693.7:c.*4218T= (CDON) ENSP00000376458.3:n.*4218T=
XM_006718950.2:c.3510A= (VSIG10L2) XP_006719013.2:n.3510A=