Canonical Allele Identifier: CA6351858

Gene: CDON

Linked Data

• ClinVar Variation Id: 2158422
• ClinVar RCV Id: RCV003093536
• dbSNP Id: rs201628624
• ExAC: 11:125871736 G / T
• gnomAD v2: 11-125871736-G-T
• gnomAD v3: 11-126001841-G-T
• gnomAD v4: 11-126001841-G-T
• MyVariant Identifiers: chr11:g.125871736G>T (hg19) ; chr11:g.126001841G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126001841G>T , CM000673.2:g.126001841G>T	GRCh38
NC_000011.9:g.125871736G>T , CM000673.1:g.125871736G>T	GRCh37
NC_000011.8:g.125376946G>T	NCBI36
NG_029776.1:g.66452C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683716.1:c.2036C>A	ENSP00000506883.1:p.Ala679Glu
ENST00000684078.1:c.2036C>A	ENSP00000507318.1:p.Ala679Glu
ENST00000684167.1:n.2435C>A
ENST00000684238.1:n.1152C>A
ENST00000684564.1:n.2246C>A
ENST00000684636.1:c.2036C>A	ENSP00000508160.1:p.Ala679Glu
ENST00000531738.6:c.2036C>A MANE Select	ENSP00000432901.2:p.Ala679Glu
ENST00000680589.1:n.554C>A
ENST00000263577.11:c.2036C>A	ENSP00000263577.7:p.Ala679Glu
ENST00000392693.7:c.2036C>A	ENSP00000376458.3:p.Ala679Glu
ENST00000531738.5:c.167C>A	ENSP00000432901.1:p.Ala56Glu
NM_001243597.1:c.2036C>A	NP_001230526.1:p.Ala679Glu
NM_016952.4:c.2036C>A	NP_058648.4:p.Ala679Glu
XM_011542862.1:c.2036C>A	XP_011541164.1:p.Ala679Glu
XM_011542863.1:c.2036C>A	XP_011541165.1:p.Ala679Glu
XM_011542864.1:c.2036C>A	XP_011541166.1:p.Ala679Glu
XM_011542865.1:c.2036C>A	XP_011541167.1:p.Ala679Glu
XM_011542866.1:c.2036C>A	XP_011541168.1:p.Ala679Glu
XM_011542862.3:c.2036C>A	XP_011541164.1:p.Ala679Glu
XM_011542863.2:c.2036C>A	XP_011541165.1:p.Ala679Glu
XM_011542864.2:c.2036C>A	XP_011541166.1:p.Ala679Glu
XM_011542865.2:c.2036C>A	XP_011541167.1:p.Ala679Glu
XM_011542866.3:c.2036C>A	XP_011541168.1:p.Ala679Glu
XM_017017873.1:c.2036C>A	XP_016873362.1:p.Ala679Glu
XR_001747899.2:n.2347C>A
NM_001243597.2:c.2036C>A	NP_001230526.1:p.Ala679Glu
NM_001378964.1:c.2036C>A MANE Select	NP_001365893.1:p.Ala679Glu
NM_016952.5:c.2036C>A	NP_058648.4:p.Ala679Glu