Canonical Allele Identifier: CA2695220032

Gene: CDAN1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42731282_42731284del , CM000677.2:g.42731282_42731284del	GRCh38
NC_000015.9:g.43023480_43023482del , CM000677.1:g.43023480_43023482del	GRCh37
NC_000015.8:g.40810772_40810774del	NCBI36
NG_012491.1:g.10938_10940del

Transcript Alleles

HGVS	Amino-acid change
ENST00000356231.4:c.1789_1791del MANE Select	ENSP00000348564.3:p.Glu597del
ENST00000643434.1:c.*967_*969del	ENSP00000494699.1:n.*967_*969del
ENST00000356231.3:c.1789_1791del	ENSP00000348564.3:p.Glu597del
NM_138477.2:c.1789_1791del	NP_612486.2:p.Glu597del
XM_005254176.3:c.1792_1794del	XP_005254233.1:p.Glu598del
XM_011521270.1:c.1816_1818del	XP_011519572.1:p.Glu606del
XM_011521271.1:c.1813_1815del	XP_011519573.1:p.Glu605del
XM_011521272.1:c.1816_1818del	XP_011519574.1:p.Glu606del
XM_011521273.1:c.1816_1818del	XP_011519575.1:p.Glu606del
XM_011521274.1:c.781_783del	XP_011519576.1:p.Glu261del
XM_011521275.1:c.1033_1035del	XP_011519577.1:p.Glu345del
XR_931757.1:n.1827_1829del
NM_138477.4:c.1789_1791del MANE Select	NP_612486.2:p.Glu597del
XM_005254176.5:c.1792_1794del	XP_005254233.1:p.Glu598del
XM_011521270.2:c.1816_1818del	XP_011519572.1:p.Glu606del
XM_011521271.2:c.1813_1815del	XP_011519573.1:p.Glu605del
XM_011521274.2:c.781_783del	XP_011519576.1:p.Glu261del
XR_001751104.1:n.1846_1848del
XR_001751105.1:n.1846_1848del
XR_931757.2:n.1847_1849del