Canonical Allele Identifier: CA13494554

Gene: CDON

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126055583C>T , CM000673.2:g.126055583C>T	GRCh38
NC_000011.9:g.125925478C>T , CM000673.1:g.125925478C>T	GRCh37
NC_000011.8:g.125430688C>T	NCBI36
NG_029776.1:g.12710G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682450.1:n.195+3650G>A
ENST00000682556.1:n.145+6996G>A
ENST00000682834.1:n.128+6996G>A
ENST00000683716.1:c.-62+6996G>A	ENSP00000506883.1:n.-62+6996G>A
ENST00000684078.1:c.-62+7689G>A	ENSP00000507318.1:n.-62+7689G>A
ENST00000684564.1:n.149+6996G>A
ENST00000684636.1:c.-62+6996G>A	ENSP00000508160.1:n.-62+6996G>A
ENST00000525625.2:n.28+6705G>A
ENST00000531738.6:c.-62+6996G>A MANE Select	ENSP00000432901.2:n.-62+6996G>A
ENST00000263577.11:c.-62+7643G>A	ENSP00000263577.7:n.-62+7643G>A
ENST00000392693.7:c.-62+7643G>A	ENSP00000376458.3:n.-62+7643G>A
ENST00000527967.5:c.-62+6996G>A	ENSP00000436940.1:n.-62+6996G>A
ENST00000531586.5:c.-62+7643G>A	ENSP00000434212.1:n.-62+7643G>A
ENST00000534818.1:c.-62+7689G>A	ENSP00000437176.1:n.-62+7689G>A
NM_001243597.1:c.-62+7643G>A	NP_001230526.1:n.-62+7643G>A
NM_016952.4:c.-62+7643G>A	NP_058648.4:n.-62+7643G>A
XM_011542862.1:c.-62+6996G>A	XP_011541164.1:n.-62+6996G>A
XM_011542863.1:c.-62+3650G>A	XP_011541165.1:n.-62+3650G>A
XM_011542864.1:c.-62+7026G>A	XP_011541166.1:n.-62+7026G>A
XM_011542865.1:c.-62+6705G>A	XP_011541167.1:n.-62+6705G>A
XM_011542866.1:c.-62+6996G>A	XP_011541168.1:n.-62+6996G>A
XM_011542862.3:c.-62+6996G>A	XP_011541164.1:n.-62+6996G>A
XM_011542863.2:c.-62+3650G>A	XP_011541165.1:n.-62+3650G>A
XM_011542864.2:c.-62+7026G>A	XP_011541166.1:n.-62+7026G>A
XM_011542865.2:c.-62+6705G>A	XP_011541167.1:n.-62+6705G>A
XM_011542866.3:c.-62+6996G>A	XP_011541168.1:n.-62+6996G>A
XM_017017873.1:c.-62+7689G>A	XP_016873362.1:n.-62+7689G>A
XR_001747899.2:n.250+6996G>A
NM_001243597.2:c.-62+7643G>A	NP_001230526.1:n.-62+7643G>A
NM_001378964.1:c.-62+6996G>A MANE Select	NP_001365893.1:n.-62+6996G>A
NM_016952.5:c.-62+7643G>A	NP_058648.4:n.-62+7643G>A