Canonical Allele Identifier: CA2438976985
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652342C= , CM000685.2:g.77652342C= GRCh38
NC_000023.10:g.76907832C= , CM000685.1:g.76907832C= GRCh37
NC_000023.9:g.76794488C= NCBI36
NG_008838.2:g.138880G=
NG_008838.3:g.138928G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4329G= MANE Select ENSP00000362441.4:p.Glu1443=
ENST00000373344.9:c.4329G= ENSP00000362441.4:p.Glu1443=
ENST00000395603.7:c.4215G= ENSP00000378967.3:p.Glu1405=
ENST00000480283.5:c.*3957G= ENSP00000480196.1:n.*3957G=
NM_000489.4:c.4329G= NP_000480.3:p.Glu1443=
NM_138270.3:c.4215G= NP_612114.2:p.Glu1405=
XM_005262153.3:c.4326G= XP_005262210.2:p.Glu1442=
XM_005262154.3:c.4242G= XP_005262211.2:p.Glu1414=
XM_005262155.3:c.4212G= XP_005262212.2:p.Glu1404=
XM_005262156.3:c.4164G= XP_005262213.2:p.Glu1388=
XM_005262157.3:c.4125G= XP_005262214.2:p.Glu1375=
XM_006724666.2:c.4212G= XP_006724729.1:p.Glu1404=
XM_006724667.2:c.4050G= XP_006724730.1:p.Glu1350=
XM_006724668.2:c.4329G= XP_006724731.1:p.Glu1443=
XR_938400.1:n.4597G=
NM_000489.5:c.4329G= NP_000480.3:p.Glu1443=
XM_005262153.5:c.4326G= XP_005262210.2:p.Glu1442=
XM_005262154.5:c.4242G= XP_005262211.2:p.Glu1414=
XM_005262155.4:c.4212G= XP_005262212.2:p.Glu1404=
XM_005262156.4:c.4164G= XP_005262213.2:p.Glu1388=
XM_005262157.5:c.4125G= XP_005262214.2:p.Glu1375=
XM_006724666.4:c.4212G= XP_006724729.1:p.Glu1404=
XM_006724667.3:c.4050G= XP_006724730.1:p.Glu1350=
XM_006724668.3:c.4329G= XP_006724731.1:p.Glu1443=
XM_017029601.2:c.4239G= XP_016885090.1:p.Glu1413=
XM_017029602.1:c.4209G= XP_016885091.1:p.Glu1403=
XM_017029603.1:c.4161G= XP_016885092.1:p.Glu1387=
XM_017029604.2:c.4128G= XP_016885093.1:p.Glu1376=
XM_017029605.1:c.4125G= XP_016885094.1:p.Glu1375=
XM_017029606.2:c.4098G= XP_016885095.1:p.Glu1366=
XM_017029607.2:c.4095G= XP_016885096.1:p.Glu1365=
XM_017029608.2:c.4047G= XP_016885097.1:p.Glu1349=
XM_017029609.1:c.4011G= XP_016885098.1:p.Glu1337=
XM_017029610.1:c.4008G= XP_016885099.1:p.Glu1336=
XM_017029611.1:c.3963G= XP_016885100.1:p.Glu1321=
XR_001755700.2:n.4554G=
NM_138270.4:c.4215G= NP_612114.2:p.Glu1405=
NM_000489.6:c.4329G= MANE Select NP_000480.3:p.Glu1443=
NM_138270.5:c.4215G= NP_612114.2:p.Glu1405=