Canonical Allele Identifier: CA2438929042
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508435A= , CM000685.2:g.77508435A= GRCh38
NC_000023.10:g.76763913A= , CM000685.1:g.76763913A= GRCh37
NC_000023.9:g.76650569A= NCBI36
NG_008838.2:g.282787T=
NG_008838.3:g.282835T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7395T= MANE Select ENSP00000362441.4:p.Gly2465=
ENST00000675732.1:c.2493T= ENSP00000502598.1:p.Gly831=
ENST00000373344.9:c.7395T= ENSP00000362441.4:p.Gly2465=
ENST00000395603.7:c.7281T= ENSP00000378967.3:p.Gly2427=
ENST00000480283.5:c.*7023T= ENSP00000480196.1:n.*7023T=
ENST00000623706.3:n.5715T=
NM_000489.4:c.7395T= NP_000480.3:p.Gly2465=
NM_138270.3:c.7281T= NP_612114.2:p.Gly2427=
XM_005262153.3:c.7392T= XP_005262210.2:p.Gly2464=
XM_005262154.3:c.7308T= XP_005262211.2:p.Gly2436=
XM_005262155.3:c.7278T= XP_005262212.2:p.Gly2426=
XM_005262156.3:c.7230T= XP_005262213.2:p.Gly2410=
XM_005262157.3:c.7191T= XP_005262214.2:p.Gly2397=
XM_006724666.2:c.7278T= XP_006724729.1:p.Gly2426=
XM_006724667.2:c.7116T= XP_006724730.1:p.Gly2372=
XR_938400.1:n.8987T=
NM_000489.5:c.7395T= NP_000480.3:p.Gly2465=
XM_005262153.5:c.7392T= XP_005262210.2:p.Gly2464=
XM_005262154.5:c.7308T= XP_005262211.2:p.Gly2436=
XM_005262155.4:c.7278T= XP_005262212.2:p.Gly2426=
XM_005262156.4:c.7230T= XP_005262213.2:p.Gly2410=
XM_005262157.5:c.7191T= XP_005262214.2:p.Gly2397=
XM_006724666.4:c.7278T= XP_006724729.1:p.Gly2426=
XM_006724667.3:c.7116T= XP_006724730.1:p.Gly2372=
XM_017029601.2:c.7305T= XP_016885090.1:p.Gly2435=
XM_017029602.1:c.7275T= XP_016885091.1:p.Gly2425=
XM_017029603.1:c.7227T= XP_016885092.1:p.Gly2409=
XM_017029604.2:c.7194T= XP_016885093.1:p.Gly2398=
XM_017029605.1:c.7191T= XP_016885094.1:p.Gly2397=
XM_017029606.2:c.7164T= XP_016885095.1:p.Gly2388=
XM_017029607.2:c.7161T= XP_016885096.1:p.Gly2387=
XM_017029608.2:c.7113T= XP_016885097.1:p.Gly2371=
XM_017029609.1:c.7077T= XP_016885098.1:p.Gly2359=
XM_017029610.1:c.7074T= XP_016885099.1:p.Gly2358=
XM_017029611.1:c.7029T= XP_016885100.1:p.Gly2343=
XR_001755700.2:n.7694T=
NM_138270.4:c.7281T= NP_612114.2:p.Gly2427=
NM_000489.6:c.7395T= MANE Select NP_000480.3:p.Gly2465=
NM_138270.5:c.7281T= NP_612114.2:p.Gly2427=