Canonical Allele Identifier: CA2438929065
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508534T= , CM000685.2:g.77508534T= GRCh38
NC_000023.10:g.76764012T= , CM000685.1:g.76764012T= GRCh37
NC_000023.9:g.76650668T= NCBI36
NG_008838.2:g.282688A=
NG_008838.3:g.282736A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7296A= MANE Select ENSP00000362441.4:p.Thr2432=
ENST00000675732.1:c.2394A= ENSP00000502598.1:p.Thr798=
ENST00000373344.9:c.7296A= ENSP00000362441.4:p.Thr2432=
ENST00000395603.7:c.7182A= ENSP00000378967.3:p.Thr2394=
ENST00000480283.5:c.*6924A= ENSP00000480196.1:n.*6924A=
ENST00000623706.3:n.5616A=
ENST00000624766.1:n.527A=
NM_000489.4:c.7296A= NP_000480.3:p.Thr2432=
NM_138270.3:c.7182A= NP_612114.2:p.Thr2394=
XM_005262153.3:c.7293A= XP_005262210.2:p.Thr2431=
XM_005262154.3:c.7209A= XP_005262211.2:p.Thr2403=
XM_005262155.3:c.7179A= XP_005262212.2:p.Thr2393=
XM_005262156.3:c.7131A= XP_005262213.2:p.Thr2377=
XM_005262157.3:c.7092A= XP_005262214.2:p.Thr2364=
XM_006724666.2:c.7179A= XP_006724729.1:p.Thr2393=
XM_006724667.2:c.7017A= XP_006724730.1:p.Thr2339=
XR_938400.1:n.8888A=
NM_000489.5:c.7296A= NP_000480.3:p.Thr2432=
XM_005262153.5:c.7293A= XP_005262210.2:p.Thr2431=
XM_005262154.5:c.7209A= XP_005262211.2:p.Thr2403=
XM_005262155.4:c.7179A= XP_005262212.2:p.Thr2393=
XM_005262156.4:c.7131A= XP_005262213.2:p.Thr2377=
XM_005262157.5:c.7092A= XP_005262214.2:p.Thr2364=
XM_006724666.4:c.7179A= XP_006724729.1:p.Thr2393=
XM_006724667.3:c.7017A= XP_006724730.1:p.Thr2339=
XM_017029601.2:c.7206A= XP_016885090.1:p.Thr2402=
XM_017029602.1:c.7176A= XP_016885091.1:p.Thr2392=
XM_017029603.1:c.7128A= XP_016885092.1:p.Thr2376=
XM_017029604.2:c.7095A= XP_016885093.1:p.Thr2365=
XM_017029605.1:c.7092A= XP_016885094.1:p.Thr2364=
XM_017029606.2:c.7065A= XP_016885095.1:p.Thr2355=
XM_017029607.2:c.7062A= XP_016885096.1:p.Thr2354=
XM_017029608.2:c.7014A= XP_016885097.1:p.Thr2338=
XM_017029609.1:c.6978A= XP_016885098.1:p.Thr2326=
XM_017029610.1:c.6975A= XP_016885099.1:p.Thr2325=
XM_017029611.1:c.6930A= XP_016885100.1:p.Thr2310=
XR_001755700.2:n.7595A=
NM_138270.4:c.7182A= NP_612114.2:p.Thr2394=
NM_000489.6:c.7296A= MANE Select NP_000480.3:p.Thr2432=
NM_138270.5:c.7182A= NP_612114.2:p.Thr2394=