Canonical Allele Identifier: CA2438933080
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77520915C= , CM000685.2:g.77520915C= GRCh38
NC_000023.10:g.76776393C= , CM000685.1:g.76776393C= GRCh37
NC_000023.9:g.76663049C= NCBI36
NG_008838.2:g.270307G=
NG_008838.3:g.270355G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7073G= MANE Select ENSP00000362441.4:p.Trp2358=
ENST00000675732.1:c.2171G= ENSP00000502598.1:p.Trp724=
ENST00000373344.9:c.7073G= ENSP00000362441.4:p.Trp2358=
ENST00000395603.7:c.6959G= ENSP00000378967.3:p.Trp2320=
ENST00000480283.5:c.*6701G= ENSP00000480196.1:n.*6701G=
ENST00000623706.3:n.5393G=
ENST00000624766.1:n.304G=
NM_000489.4:c.7073G= NP_000480.3:p.Trp2358=
NM_138270.3:c.6959G= NP_612114.2:p.Trp2320=
XM_005262153.3:c.7070G= XP_005262210.2:p.Trp2357=
XM_005262154.3:c.6986G= XP_005262211.2:p.Trp2329=
XM_005262155.3:c.6956G= XP_005262212.2:p.Trp2319=
XM_005262156.3:c.6908G= XP_005262213.2:p.Trp2303=
XM_005262157.3:c.6869G= XP_005262214.2:p.Trp2290=
XM_006724666.2:c.6956G= XP_006724729.1:p.Trp2319=
XM_006724667.2:c.6794G= XP_006724730.1:p.Trp2265=
XR_938400.1:n.8665G=
NM_000489.5:c.7073G= NP_000480.3:p.Trp2358=
XM_005262153.5:c.7070G= XP_005262210.2:p.Trp2357=
XM_005262154.5:c.6986G= XP_005262211.2:p.Trp2329=
XM_005262155.4:c.6956G= XP_005262212.2:p.Trp2319=
XM_005262156.4:c.6908G= XP_005262213.2:p.Trp2303=
XM_005262157.5:c.6869G= XP_005262214.2:p.Trp2290=
XM_006724666.4:c.6956G= XP_006724729.1:p.Trp2319=
XM_006724667.3:c.6794G= XP_006724730.1:p.Trp2265=
XM_017029601.2:c.6983G= XP_016885090.1:p.Trp2328=
XM_017029602.1:c.6953G= XP_016885091.1:p.Trp2318=
XM_017029603.1:c.6905G= XP_016885092.1:p.Trp2302=
XM_017029604.2:c.6872G= XP_016885093.1:p.Trp2291=
XM_017029605.1:c.6869G= XP_016885094.1:p.Trp2290=
XM_017029606.2:c.6842G= XP_016885095.1:p.Trp2281=
XM_017029607.2:c.6839G= XP_016885096.1:p.Trp2280=
XM_017029608.2:c.6791G= XP_016885097.1:p.Trp2264=
XM_017029609.1:c.6755G= XP_016885098.1:p.Trp2252=
XM_017029610.1:c.6752G= XP_016885099.1:p.Trp2251=
XM_017029611.1:c.6707G= XP_016885100.1:p.Trp2236=
XR_001755700.2:n.7372G=
NM_138270.4:c.6959G= NP_612114.2:p.Trp2320=
NM_000489.6:c.7073G= MANE Select NP_000480.3:p.Trp2358=
NM_138270.5:c.6959G= NP_612114.2:p.Trp2320=