Canonical Allele Identifier: CA230548845
Gene: CDON HGNC NCBI
VSIG10L2 HGNC NCBI

Linked Data

dbSNP Id: rs1019842620
gnomAD v2: 11-125826705-TAAG-T
gnomAD v3: 11-125956810-TAAG-T
gnomAD v4: 11-125956810-TAAG-T
MyVariant Identifiers: chr11:g.125826706_125826708del (hg19) chr11:g.125956811_125956813del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.125956815_125956817del , CM000673.2:g.125956815_125956817del GRCh38
NC_000011.9:g.125826710_125826712del , CM000673.1:g.125826710_125826712del GRCh37
NC_000011.8:g.125331920_125331922del NCBI36
NG_029776.1:g.111480_111482del

Transcript Alleles

HGVS Amino-acid change
ENST00000684078.1:c.*4129_*4131del (CDON) ENSP00000507318.1:n.*4129_*4131del
ENST00000638636.2:c.3205_3207del (VSIG10L2) ENSP00000491467.1:n.3205_3207del
ENST00000392693.7:c.*4129_*4131del (CDON) ENSP00000376458.3:n.*4129_*4131del
XM_006718950.2:c.3601_3603del (VSIG10L2) XP_006719013.2:n.3601_3603del
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