Canonical Allele Identifier: CA2438987780
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77684427C= , CM000685.2:g.77684427C= GRCh38
NC_000023.10:g.76939919C= , CM000685.1:g.76939919C= GRCh37
NC_000023.9:g.76826575C= NCBI36
NG_008838.2:g.106795G=
NG_008838.3:g.106843G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.829G= MANE Select ENSP00000362441.4:p.Val277=
ENST00000373344.9:c.829G= ENSP00000362441.4:p.Val277=
ENST00000395603.7:c.715G= ENSP00000378967.3:p.Val239=
ENST00000480283.5:c.*457G= ENSP00000480196.1:n.*457G=
ENST00000623321.3:c.664G= ENSP00000485127.1:p.Val222=
ENST00000624032.3:c.829G= ENSP00000485253.1:p.Val277=
ENST00000624166.3:c.712G= ENSP00000485103.1:p.Val238=
NM_000489.4:c.829G= NP_000480.3:p.Val277=
NM_138270.3:c.715G= NP_612114.2:p.Val239=
XM_005262153.3:c.826G= XP_005262210.2:p.Val276=
XM_005262154.3:c.829G= XP_005262211.2:p.Val277=
XM_005262155.3:c.712G= XP_005262212.2:p.Val238=
XM_005262156.3:c.664G= XP_005262213.2:p.Val222=
XM_005262157.3:c.712G= XP_005262214.2:p.Val238=
XM_006724666.2:c.712G= XP_006724729.1:p.Val238=
XM_006724667.2:c.550G= XP_006724730.1:p.Val184=
XM_006724668.2:c.829G= XP_006724731.1:p.Val277=
XR_938400.1:n.1097G=
NM_000489.5:c.829G= NP_000480.3:p.Val277=
XM_005262153.5:c.826G= XP_005262210.2:p.Val276=
XM_005262154.5:c.829G= XP_005262211.2:p.Val277=
XM_005262155.4:c.712G= XP_005262212.2:p.Val238=
XM_005262156.4:c.664G= XP_005262213.2:p.Val222=
XM_005262157.5:c.712G= XP_005262214.2:p.Val238=
XM_006724666.4:c.712G= XP_006724729.1:p.Val238=
XM_006724667.3:c.550G= XP_006724730.1:p.Val184=
XM_006724668.3:c.829G= XP_006724731.1:p.Val277=
XM_017029601.2:c.826G= XP_016885090.1:p.Val276=
XM_017029602.1:c.709G= XP_016885091.1:p.Val237=
XM_017029603.1:c.661G= XP_016885092.1:p.Val221=
XM_017029604.2:c.715G= XP_016885093.1:p.Val239=
XM_017029605.1:c.712G= XP_016885094.1:p.Val238=
XM_017029606.2:c.598G= XP_016885095.1:p.Val200=
XM_017029607.2:c.595G= XP_016885096.1:p.Val199=
XM_017029608.2:c.547G= XP_016885097.1:p.Val183=
XM_017029609.1:c.598G= XP_016885098.1:p.Val200=
XM_017029610.1:c.595G= XP_016885099.1:p.Val199=
XM_017029611.1:c.550G= XP_016885100.1:p.Val184=
XR_001755700.2:n.1054G=
NM_138270.4:c.715G= NP_612114.2:p.Val239=
NM_000489.6:c.829G= MANE Select NP_000480.3:p.Val277=
NM_138270.5:c.715G= NP_612114.2:p.Val239=