Canonical Allele Identifier: CA2438929032
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508409C= , CM000685.2:g.77508409C= GRCh38
NC_000023.10:g.76763887C= , CM000685.1:g.76763887C= GRCh37
NC_000023.9:g.76650543C= NCBI36
NG_008838.2:g.282813G=
NG_008838.3:g.282861G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7421G= MANE Select ENSP00000362441.4:p.Arg2474=
ENST00000675732.1:c.2519G= ENSP00000502598.1:p.Arg840=
ENST00000373344.9:c.7421G= ENSP00000362441.4:p.Arg2474=
ENST00000395603.7:c.7307G= ENSP00000378967.3:p.Arg2436=
ENST00000480283.5:c.*7049G= ENSP00000480196.1:n.*7049G=
ENST00000623706.3:n.5741G=
NM_000489.4:c.7421G= NP_000480.3:p.Arg2474=
NM_138270.3:c.7307G= NP_612114.2:p.Arg2436=
XM_005262153.3:c.7418G= XP_005262210.2:p.Arg2473=
XM_005262154.3:c.7334G= XP_005262211.2:p.Arg2445=
XM_005262155.3:c.7304G= XP_005262212.2:p.Arg2435=
XM_005262156.3:c.7256G= XP_005262213.2:p.Arg2419=
XM_005262157.3:c.7217G= XP_005262214.2:p.Arg2406=
XM_006724666.2:c.7304G= XP_006724729.1:p.Arg2435=
XM_006724667.2:c.7142G= XP_006724730.1:p.Arg2381=
XR_938400.1:n.9013G=
NM_000489.5:c.7421G= NP_000480.3:p.Arg2474=
XM_005262153.5:c.7418G= XP_005262210.2:p.Arg2473=
XM_005262154.5:c.7334G= XP_005262211.2:p.Arg2445=
XM_005262155.4:c.7304G= XP_005262212.2:p.Arg2435=
XM_005262156.4:c.7256G= XP_005262213.2:p.Arg2419=
XM_005262157.5:c.7217G= XP_005262214.2:p.Arg2406=
XM_006724666.4:c.7304G= XP_006724729.1:p.Arg2435=
XM_006724667.3:c.7142G= XP_006724730.1:p.Arg2381=
XM_017029601.2:c.7331G= XP_016885090.1:p.Arg2444=
XM_017029602.1:c.7301G= XP_016885091.1:p.Arg2434=
XM_017029603.1:c.7253G= XP_016885092.1:p.Arg2418=
XM_017029604.2:c.7220G= XP_016885093.1:p.Arg2407=
XM_017029605.1:c.7217G= XP_016885094.1:p.Arg2406=
XM_017029606.2:c.7190G= XP_016885095.1:p.Arg2397=
XM_017029607.2:c.7187G= XP_016885096.1:p.Arg2396=
XM_017029608.2:c.7139G= XP_016885097.1:p.Arg2380=
XM_017029609.1:c.7103G= XP_016885098.1:p.Arg2368=
XM_017029610.1:c.7100G= XP_016885099.1:p.Arg2367=
XM_017029611.1:c.7055G= XP_016885100.1:p.Arg2352=
XR_001755700.2:n.7720G=
NM_138270.4:c.7307G= NP_612114.2:p.Arg2436=
NM_000489.6:c.7421G= MANE Select NP_000480.3:p.Arg2474=
NM_138270.5:c.7307G= NP_612114.2:p.Arg2436=