Canonical Allele Identifier: CA2616706255

Gene: CDON VSIG10L2

Linked Data

• gnomAD v4: 11-125956816-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.125956816G>T , CM000673.2:g.125956816G>T	GRCh38
NC_000011.9:g.125826711G>T , CM000673.1:g.125826711G>T	GRCh37
NC_000011.8:g.125331921G>T	NCBI36
NG_029776.1:g.111477C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000684078.1:c.*4126C>A (CDON)	ENSP00000507318.1:n.*4126C>A
ENST00000638636.2:c.3206G>T (VSIG10L2)	ENSP00000491467.1:n.3206G>T
ENST00000392693.7:c.*4126C>A (CDON)	ENSP00000376458.3:n.*4126C>A
XM_006718950.2:c.3602G>T (VSIG10L2)	XP_006719013.2:n.3602G>T
XM_011542862.3:c.*4126C>A (CDON)	XP_011541164.1:n.*4126C>A
XM_011542863.2:c.*4126C>A (CDON)	XP_011541165.1:n.*4126C>A
XM_011542864.2:c.*4126C>A (CDON)	XP_011541166.1:n.*4126C>A
XM_011542865.2:c.*4126C>A (CDON)	XP_011541167.1:n.*4126C>A
XM_011542866.3:c.*4126C>A (CDON)	XP_011541168.1:n.*4126C>A
XM_017017873.1:c.*4126C>A (CDON)	XP_016873362.1:n.*4126C>A
XR_001747899.2:n.8239C>A (CDON)