Canonical Allele Identifier: CA673038337

Gene: CDON

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126003207G>T , CM000673.2:g.126003207G>T	GRCh38
NC_000011.9:g.125873102G>T , CM000673.1:g.125873102G>T	GRCh37
NC_000011.8:g.125378312G>T	NCBI36
NG_029776.1:g.65086C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683716.1:c.2026+695C>A	ENSP00000506883.1:n.2026+695C>A
ENST00000684078.1:c.2026+695C>A	ENSP00000507318.1:n.2026+695C>A
ENST00000684167.1:n.2425+695C>A
ENST00000684238.1:n.1142+695C>A
ENST00000684564.1:n.2236+695C>A
ENST00000684636.1:c.2026+695C>A	ENSP00000508160.1:n.2026+695C>A
ENST00000531738.6:c.2026+695C>A MANE Select	ENSP00000432901.2:n.2026+695C>A
ENST00000680589.1:n.544+695C>A
ENST00000263577.11:c.2026+695C>A	ENSP00000263577.7:n.2026+695C>A
ENST00000392693.7:c.2026+695C>A	ENSP00000376458.3:n.2026+695C>A
ENST00000531738.5:c.157+695C>A	ENSP00000432901.1:n.157+695C>A
NM_001243597.1:c.2026+695C>A	NP_001230526.1:n.2026+695C>A
NM_016952.4:c.2026+695C>A	NP_058648.4:n.2026+695C>A
XM_011542862.1:c.2026+695C>A	XP_011541164.1:n.2026+695C>A
XM_011542863.1:c.2026+695C>A	XP_011541165.1:n.2026+695C>A
XM_011542864.1:c.2026+695C>A	XP_011541166.1:n.2026+695C>A
XM_011542865.1:c.2026+695C>A	XP_011541167.1:n.2026+695C>A
XM_011542866.1:c.2026+695C>A	XP_011541168.1:n.2026+695C>A
XM_011542862.3:c.2026+695C>A	XP_011541164.1:n.2026+695C>A
XM_011542863.2:c.2026+695C>A	XP_011541165.1:n.2026+695C>A
XM_011542864.2:c.2026+695C>A	XP_011541166.1:n.2026+695C>A
XM_011542865.2:c.2026+695C>A	XP_011541167.1:n.2026+695C>A
XM_011542866.3:c.2026+695C>A	XP_011541168.1:n.2026+695C>A
XM_017017873.1:c.2026+695C>A	XP_016873362.1:n.2026+695C>A
XR_001747899.2:n.2337+695C>A
NM_001243597.2:c.2026+695C>A	NP_001230526.1:n.2026+695C>A
NM_001378964.1:c.2026+695C>A MANE Select	NP_001365893.1:n.2026+695C>A
NM_016952.5:c.2026+695C>A	NP_058648.4:n.2026+695C>A