Canonical Allele Identifier: CA2616706153
Gene: CDON HGNC NCBI
VSIG10L2 HGNC NCBI

Linked Data

gnomAD v4: 11-125956719-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.125956719C>T , CM000673.2:g.125956719C>T GRCh38
NC_000011.9:g.125826614C>T , CM000673.1:g.125826614C>T GRCh37
NC_000011.8:g.125331824C>T NCBI36
NG_029776.1:g.111574G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684078.1:c.*4223G>A (CDON) ENSP00000507318.1:n.*4223G>A
ENST00000638636.2:c.3109C>T (VSIG10L2) ENSP00000491467.1:n.3109C>T
ENST00000392693.7:c.*4223G>A (CDON) ENSP00000376458.3:n.*4223G>A
XM_006718950.2:c.3505C>T (VSIG10L2) XP_006719013.2:n.3505C>T
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