Canonical Allele Identifier: CA2438929063
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508529C= , CM000685.2:g.77508529C= GRCh38
NC_000023.10:g.76764007C= , CM000685.1:g.76764007C= GRCh37
NC_000023.9:g.76650663C= NCBI36
NG_008838.2:g.282693G=
NG_008838.3:g.282741G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7301G= MANE Select ENSP00000362441.4:p.Gly2434=
ENST00000675732.1:c.2399G= ENSP00000502598.1:p.Gly800=
ENST00000373344.9:c.7301G= ENSP00000362441.4:p.Gly2434=
ENST00000395603.7:c.7187G= ENSP00000378967.3:p.Gly2396=
ENST00000480283.5:c.*6929G= ENSP00000480196.1:n.*6929G=
ENST00000623706.3:n.5621G=
ENST00000624766.1:n.532G=
NM_000489.4:c.7301G= NP_000480.3:p.Gly2434=
NM_138270.3:c.7187G= NP_612114.2:p.Gly2396=
XM_005262153.3:c.7298G= XP_005262210.2:p.Gly2433=
XM_005262154.3:c.7214G= XP_005262211.2:p.Gly2405=
XM_005262155.3:c.7184G= XP_005262212.2:p.Gly2395=
XM_005262156.3:c.7136G= XP_005262213.2:p.Gly2379=
XM_005262157.3:c.7097G= XP_005262214.2:p.Gly2366=
XM_006724666.2:c.7184G= XP_006724729.1:p.Gly2395=
XM_006724667.2:c.7022G= XP_006724730.1:p.Gly2341=
XR_938400.1:n.8893G=
NM_000489.5:c.7301G= NP_000480.3:p.Gly2434=
XM_005262153.5:c.7298G= XP_005262210.2:p.Gly2433=
XM_005262154.5:c.7214G= XP_005262211.2:p.Gly2405=
XM_005262155.4:c.7184G= XP_005262212.2:p.Gly2395=
XM_005262156.4:c.7136G= XP_005262213.2:p.Gly2379=
XM_005262157.5:c.7097G= XP_005262214.2:p.Gly2366=
XM_006724666.4:c.7184G= XP_006724729.1:p.Gly2395=
XM_006724667.3:c.7022G= XP_006724730.1:p.Gly2341=
XM_017029601.2:c.7211G= XP_016885090.1:p.Gly2404=
XM_017029602.1:c.7181G= XP_016885091.1:p.Gly2394=
XM_017029603.1:c.7133G= XP_016885092.1:p.Gly2378=
XM_017029604.2:c.7100G= XP_016885093.1:p.Gly2367=
XM_017029605.1:c.7097G= XP_016885094.1:p.Gly2366=
XM_017029606.2:c.7070G= XP_016885095.1:p.Gly2357=
XM_017029607.2:c.7067G= XP_016885096.1:p.Gly2356=
XM_017029608.2:c.7019G= XP_016885097.1:p.Gly2340=
XM_017029609.1:c.6983G= XP_016885098.1:p.Gly2328=
XM_017029610.1:c.6980G= XP_016885099.1:p.Gly2327=
XM_017029611.1:c.6935G= XP_016885100.1:p.Gly2312=
XR_001755700.2:n.7600G=
NM_138270.4:c.7187G= NP_612114.2:p.Gly2396=
NM_000489.6:c.7301G= MANE Select NP_000480.3:p.Gly2434=
NM_138270.5:c.7187G= NP_612114.2:p.Gly2396=