Canonical Allele Identifier: CA2438976924
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652306C= , CM000685.2:g.77652306C= GRCh38
NC_000023.10:g.76907796C= , CM000685.1:g.76907796C= GRCh37
NC_000023.9:g.76794452C= NCBI36
NG_008838.2:g.138916G=
NG_008838.3:g.138964G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4365G= MANE Select ENSP00000362441.4:p.Glu1455=
ENST00000373344.9:c.4365G= ENSP00000362441.4:p.Glu1455=
ENST00000395603.7:c.4251G= ENSP00000378967.3:p.Glu1417=
ENST00000480283.5:c.*3993G= ENSP00000480196.1:n.*3993G=
NM_000489.4:c.4365G= NP_000480.3:p.Glu1455=
NM_138270.3:c.4251G= NP_612114.2:p.Glu1417=
XM_005262153.3:c.4362G= XP_005262210.2:p.Glu1454=
XM_005262154.3:c.4278G= XP_005262211.2:p.Glu1426=
XM_005262155.3:c.4248G= XP_005262212.2:p.Glu1416=
XM_005262156.3:c.4200G= XP_005262213.2:p.Glu1400=
XM_005262157.3:c.4161G= XP_005262214.2:p.Glu1387=
XM_006724666.2:c.4248G= XP_006724729.1:p.Glu1416=
XM_006724667.2:c.4086G= XP_006724730.1:p.Glu1362=
XM_006724668.2:c.4365G= XP_006724731.1:p.Glu1455=
XR_938400.1:n.4633G=
NM_000489.5:c.4365G= NP_000480.3:p.Glu1455=
XM_005262153.5:c.4362G= XP_005262210.2:p.Glu1454=
XM_005262154.5:c.4278G= XP_005262211.2:p.Glu1426=
XM_005262155.4:c.4248G= XP_005262212.2:p.Glu1416=
XM_005262156.4:c.4200G= XP_005262213.2:p.Glu1400=
XM_005262157.5:c.4161G= XP_005262214.2:p.Glu1387=
XM_006724666.4:c.4248G= XP_006724729.1:p.Glu1416=
XM_006724667.3:c.4086G= XP_006724730.1:p.Glu1362=
XM_006724668.3:c.4365G= XP_006724731.1:p.Glu1455=
XM_017029601.2:c.4275G= XP_016885090.1:p.Glu1425=
XM_017029602.1:c.4245G= XP_016885091.1:p.Glu1415=
XM_017029603.1:c.4197G= XP_016885092.1:p.Glu1399=
XM_017029604.2:c.4164G= XP_016885093.1:p.Glu1388=
XM_017029605.1:c.4161G= XP_016885094.1:p.Glu1387=
XM_017029606.2:c.4134G= XP_016885095.1:p.Glu1378=
XM_017029607.2:c.4131G= XP_016885096.1:p.Glu1377=
XM_017029608.2:c.4083G= XP_016885097.1:p.Glu1361=
XM_017029609.1:c.4047G= XP_016885098.1:p.Glu1349=
XM_017029610.1:c.4044G= XP_016885099.1:p.Glu1348=
XM_017029611.1:c.3999G= XP_016885100.1:p.Glu1333=
XR_001755700.2:n.4590G=
NM_138270.4:c.4251G= NP_612114.2:p.Glu1417=
NM_000489.6:c.4365G= MANE Select NP_000480.3:p.Glu1455=
NM_138270.5:c.4251G= NP_612114.2:p.Glu1417=