Canonical Allele Identifier: CA230548854

Gene: CDON VSIG10L2

Linked Data

• dbSNP Id: rs552747570
• gnomAD v3: 11-125956826-T-C
• gnomAD v4: 11-125956826-T-C
• MyVariant Identifiers: chr11:g.125826721T>C (hg19) ; chr11:g.125956826T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.125956826T>C , CM000673.2:g.125956826T>C	GRCh38
NC_000011.9:g.125826721T>C , CM000673.1:g.125826721T>C	GRCh37
NC_000011.8:g.125331931T>C	NCBI36
NG_029776.1:g.111467A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684078.1:c.*4116A>G (CDON)	ENSP00000507318.1:n.*4116A>G
ENST00000531738.6:c.*4116A>G (CDON) MANE Select	ENSP00000432901.2:n.*4116A>G
ENST00000638636.2:c.3216T>C (VSIG10L2)	ENSP00000491467.1:n.3216T>C
ENST00000392693.7:c.*4116A>G (CDON)	ENSP00000376458.3:n.*4116A>G
NM_001243597.1:c.*4116A>G (CDON)	NP_001230526.1:n.*4116A>G
NM_016952.4:c.*4116A>G (CDON)	NP_058648.4:n.*4116A>G
XM_006718950.2:c.3612T>C (VSIG10L2)	XP_006719013.2:n.3612T>C
XM_011542866.1:c.*4116A>G (CDON)	XP_011541168.1:n.*4116A>G
XM_011542862.3:c.*4116A>G (CDON)	XP_011541164.1:n.*4116A>G
XM_011542863.2:c.*4116A>G (CDON)	XP_011541165.1:n.*4116A>G
XM_011542864.2:c.*4116A>G (CDON)	XP_011541166.1:n.*4116A>G
XM_011542865.2:c.*4116A>G (CDON)	XP_011541167.1:n.*4116A>G
XM_011542866.3:c.*4116A>G (CDON)	XP_011541168.1:n.*4116A>G
XM_017017873.1:c.*4116A>G (CDON)	XP_016873362.1:n.*4116A>G
XR_001747899.2:n.8229A>G (CDON)
NM_001243597.2:c.*4116A>G (CDON)	NP_001230526.1:n.*4116A>G
NM_001378964.1:c.*4116A>G (CDON) MANE Select	NP_001365893.1:n.*4116A>G
NM_016952.5:c.*4116A>G (CDON)	NP_058648.4:n.*4116A>G