Canonical Allele Identifier: CA2006890474
Gene: CDON HGNC NCBI
VSIG10L2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.125956808C= , CM000673.2:g.125956808C= GRCh38
NC_000011.9:g.125826703C= , CM000673.1:g.125826703C= GRCh37
NC_000011.8:g.125331913C= NCBI36
NG_029776.1:g.111485G=

Transcript Alleles

HGVS Amino-acid change
ENST00000684078.1:c.*4134G= (CDON) ENSP00000507318.1:n.*4134G=
ENST00000638636.2:c.3198C= (VSIG10L2) ENSP00000491467.1:n.3198C=
ENST00000392693.7:c.*4134G= (CDON) ENSP00000376458.3:n.*4134G=
XM_006718950.2:c.3594C= (VSIG10L2) XP_006719013.2:n.3594C=