Canonical Allele Identifier: CA2438976815
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652229C= , CM000685.2:g.77652229C= GRCh38
NC_000023.10:g.76907719C= , CM000685.1:g.76907719C= GRCh37
NC_000023.9:g.76794375C= NCBI36
NG_008838.2:g.138993G=
NG_008838.3:g.139041G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4442G= MANE Select ENSP00000362441.4:p.Arg1481=
ENST00000373344.9:c.4442G= ENSP00000362441.4:p.Arg1481=
ENST00000395603.7:c.4328G= ENSP00000378967.3:p.Arg1443=
ENST00000480283.5:c.*4070G= ENSP00000480196.1:n.*4070G=
ENST00000623242.3:c.48G=
NM_000489.4:c.4442G= NP_000480.3:p.Arg1481=
NM_138270.3:c.4328G= NP_612114.2:p.Arg1443=
XM_005262153.3:c.4439G= XP_005262210.2:p.Arg1480=
XM_005262154.3:c.4355G= XP_005262211.2:p.Arg1452=
XM_005262155.3:c.4325G= XP_005262212.2:p.Arg1442=
XM_005262156.3:c.4277G= XP_005262213.2:p.Arg1426=
XM_005262157.3:c.4238G= XP_005262214.2:p.Arg1413=
XM_006724666.2:c.4325G= XP_006724729.1:p.Arg1442=
XM_006724667.2:c.4163G= XP_006724730.1:p.Arg1388=
XM_006724668.2:c.4442G= XP_006724731.1:p.Arg1481=
XR_938400.1:n.4710G=
NM_000489.5:c.4442G= NP_000480.3:p.Arg1481=
XM_005262153.5:c.4439G= XP_005262210.2:p.Arg1480=
XM_005262154.5:c.4355G= XP_005262211.2:p.Arg1452=
XM_005262155.4:c.4325G= XP_005262212.2:p.Arg1442=
XM_005262156.4:c.4277G= XP_005262213.2:p.Arg1426=
XM_005262157.5:c.4238G= XP_005262214.2:p.Arg1413=
XM_006724666.4:c.4325G= XP_006724729.1:p.Arg1442=
XM_006724667.3:c.4163G= XP_006724730.1:p.Arg1388=
XM_006724668.3:c.4442G= XP_006724731.1:p.Arg1481=
XM_017029601.2:c.4352G= XP_016885090.1:p.Arg1451=
XM_017029602.1:c.4322G= XP_016885091.1:p.Arg1441=
XM_017029603.1:c.4274G= XP_016885092.1:p.Arg1425=
XM_017029604.2:c.4241G= XP_016885093.1:p.Arg1414=
XM_017029605.1:c.4238G= XP_016885094.1:p.Arg1413=
XM_017029606.2:c.4211G= XP_016885095.1:p.Arg1404=
XM_017029607.2:c.4208G= XP_016885096.1:p.Arg1403=
XM_017029608.2:c.4160G= XP_016885097.1:p.Arg1387=
XM_017029609.1:c.4124G= XP_016885098.1:p.Arg1375=
XM_017029610.1:c.4121G= XP_016885099.1:p.Arg1374=
XM_017029611.1:c.4076G= XP_016885100.1:p.Arg1359=
XR_001755700.2:n.4667G=
NM_138270.4:c.4328G= NP_612114.2:p.Arg1443=
NM_000489.6:c.4442G= MANE Select NP_000480.3:p.Arg1481=
NM_138270.5:c.4328G= NP_612114.2:p.Arg1443=