Canonical Allele Identifier: CA383212148

Gene: CDON

Linked Data

• MyVariant Identifiers: chr11:g.125891299C>G (hg19) ; chr11:g.126021404C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126021404C>G , CM000673.2:g.126021404C>G	GRCh38
NC_000011.9:g.125891299C>G , CM000673.1:g.125891299C>G	GRCh37
NC_000011.8:g.125396509C>G	NCBI36
NG_029776.1:g.46889G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682450.1:n.312G>C
ENST00000682556.1:n.399G>C
ENST00000682834.1:n.382G>C
ENST00000683716.1:c.193G>C	ENSP00000506883.1:p.Gly65Arg
ENST00000684078.1:c.193G>C	ENSP00000507318.1:p.Gly65Arg
ENST00000684167.1:n.599G>C
ENST00000684564.1:n.403G>C
ENST00000684636.1:c.193G>C	ENSP00000508160.1:p.Gly65Arg
ENST00000525625.2:n.282G>C
ENST00000531738.6:c.193G>C MANE Select	ENSP00000432901.2:p.Gly65Arg
ENST00000531830.2:c.117G>C
ENST00000263577.11:c.193G>C	ENSP00000263577.7:p.Gly65Arg
ENST00000392693.7:c.193G>C	ENSP00000376458.3:p.Gly65Arg
ENST00000525625.1:n.256G>C
ENST00000527967.5:c.193G>C	ENSP00000436940.1:p.Gly65Arg
ENST00000531586.5:c.193G>C	ENSP00000434212.1:p.Gly65Arg
ENST00000534661.5:c.119G>C
ENST00000534818.1:c.193G>C	ENSP00000437176.1:p.Gly65Arg
NM_001243597.1:c.193G>C	NP_001230526.1:p.Gly65Arg
NM_016952.4:c.193G>C	NP_058648.4:p.Gly65Arg
XM_011542862.1:c.193G>C	XP_011541164.1:p.Gly65Arg
XM_011542863.1:c.193G>C	XP_011541165.1:p.Gly65Arg
XM_011542864.1:c.193G>C	XP_011541166.1:p.Gly65Arg
XM_011542865.1:c.193G>C	XP_011541167.1:p.Gly65Arg
XM_011542866.1:c.193G>C	XP_011541168.1:p.Gly65Arg
XM_011542862.3:c.193G>C	XP_011541164.1:p.Gly65Arg
XM_011542863.2:c.193G>C	XP_011541165.1:p.Gly65Arg
XM_011542864.2:c.193G>C	XP_011541166.1:p.Gly65Arg
XM_011542865.2:c.193G>C	XP_011541167.1:p.Gly65Arg
XM_011542866.3:c.193G>C	XP_011541168.1:p.Gly65Arg
XM_017017873.1:c.193G>C	XP_016873362.1:p.Gly65Arg
XR_001747899.2:n.504G>C
NM_001243597.2:c.193G>C	NP_001230526.1:p.Gly65Arg
NM_001378964.1:c.193G>C MANE Select	NP_001365893.1:p.Gly65Arg
NM_016952.5:c.193G>C	NP_058648.4:p.Gly65Arg