Canonical Allele Identifier: CA2738745655

Gene: ATRX

Linked Data

• dbSNP Id: rs2148440481

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652342_77652344del , CM000685.2:g.77652342_77652344del	GRCh38
NC_000023.10:g.76907832_76907834del , CM000685.1:g.76907832_76907834del	GRCh37
NC_000023.9:g.76794488_76794490del	NCBI36
NG_008838.2:g.138880_138882del
NG_008838.3:g.138928_138930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4329_4331del MANE Select	ENSP00000362441.4:p.Glu1444del
ENST00000373344.9:c.4329_4331del	ENSP00000362441.4:p.Glu1444del
ENST00000395603.7:c.4215_4217del	ENSP00000378967.3:p.Glu1406del
ENST00000480283.5:c.*3957_*3959del	ENSP00000480196.1:n.*3957_*3959del
NM_000489.4:c.4329_4331del	NP_000480.3:p.Glu1444del
NM_138270.3:c.4215_4217del	NP_612114.2:p.Glu1406del
XM_005262153.3:c.4326_4328del	XP_005262210.2:p.Glu1443del
XM_005262154.3:c.4242_4244del	XP_005262211.2:p.Glu1415del
XM_005262155.3:c.4212_4214del	XP_005262212.2:p.Glu1405del
XM_005262156.3:c.4164_4166del	XP_005262213.2:p.Glu1389del
XM_005262157.3:c.4125_4127del	XP_005262214.2:p.Glu1376del
XM_006724666.2:c.4212_4214del	XP_006724729.1:p.Glu1405del
XM_006724667.2:c.4050_4052del	XP_006724730.1:p.Glu1351del
XM_006724668.2:c.4329_4331del	XP_006724731.1:p.Glu1444del
XR_938400.1:n.4597_4599del
NM_000489.5:c.4329_4331del	NP_000480.3:p.Glu1444del
XM_005262153.5:c.4326_4328del	XP_005262210.2:p.Glu1443del
XM_005262154.5:c.4242_4244del	XP_005262211.2:p.Glu1415del
XM_005262155.4:c.4212_4214del	XP_005262212.2:p.Glu1405del
XM_005262156.4:c.4164_4166del	XP_005262213.2:p.Glu1389del
XM_005262157.5:c.4125_4127del	XP_005262214.2:p.Glu1376del
XM_006724666.4:c.4212_4214del	XP_006724729.1:p.Glu1405del
XM_006724667.3:c.4050_4052del	XP_006724730.1:p.Glu1351del
XM_006724668.3:c.4329_4331del	XP_006724731.1:p.Glu1444del
XM_017029601.2:c.4239_4241del	XP_016885090.1:p.Glu1414del
XM_017029602.1:c.4209_4211del	XP_016885091.1:p.Glu1404del
XM_017029603.1:c.4161_4163del	XP_016885092.1:p.Glu1388del
XM_017029604.2:c.4128_4130del	XP_016885093.1:p.Glu1377del
XM_017029605.1:c.4125_4127del	XP_016885094.1:p.Glu1376del
XM_017029606.2:c.4098_4100del	XP_016885095.1:p.Glu1367del
XM_017029607.2:c.4095_4097del	XP_016885096.1:p.Glu1366del
XM_017029608.2:c.4047_4049del	XP_016885097.1:p.Glu1350del
XM_017029609.1:c.4011_4013del	XP_016885098.1:p.Glu1338del
XM_017029610.1:c.4008_4010del	XP_016885099.1:p.Glu1337del
XM_017029611.1:c.3963_3965del	XP_016885100.1:p.Glu1322del
XR_001755700.2:n.4554_4556del
NM_138270.4:c.4215_4217del	NP_612114.2:p.Glu1406del
NM_000489.6:c.4329_4331del MANE Select	NP_000480.3:p.Glu1444del
NM_138270.5:c.4215_4217del	NP_612114.2:p.Glu1406del