Canonical Allele Identifier: CA2438933064
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77520838C= , CM000685.2:g.77520838C= GRCh38
NC_000023.10:g.76776316C= , CM000685.1:g.76776316C= GRCh37
NC_000023.9:g.76662972C= NCBI36
NG_008838.2:g.270384G=
NG_008838.3:g.270432G=

Transcript Alleles

HGVS Amino-acid change
ENST00000373344.11:c.7150G= MANE Select ENSP00000362441.4:p.Val2384=
ENST00000675732.1:c.2248G= ENSP00000502598.1:p.Val750=
ENST00000373344.9:c.7150G= ENSP00000362441.4:p.Val2384=
ENST00000395603.7:c.7036G= ENSP00000378967.3:p.Val2346=
ENST00000480283.5:c.*6778G= ENSP00000480196.1:n.*6778G=
ENST00000623706.3:n.5470G=
ENST00000624766.1:n.381G=
NM_000489.4:c.7150G= NP_000480.3:p.Val2384=
NM_138270.3:c.7036G= NP_612114.2:p.Val2346=
XM_005262153.3:c.7147G= XP_005262210.2:p.Val2383=
XM_005262154.3:c.7063G= XP_005262211.2:p.Val2355=
XM_005262155.3:c.7033G= XP_005262212.2:p.Val2345=
XM_005262156.3:c.6985G= XP_005262213.2:p.Val2329=
XM_005262157.3:c.6946G= XP_005262214.2:p.Val2316=
XM_006724666.2:c.7033G= XP_006724729.1:p.Val2345=
XM_006724667.2:c.6871G= XP_006724730.1:p.Val2291=
XR_938400.1:n.8742G=
NM_000489.5:c.7150G= NP_000480.3:p.Val2384=
XM_005262153.5:c.7147G= XP_005262210.2:p.Val2383=
XM_005262154.5:c.7063G= XP_005262211.2:p.Val2355=
XM_005262155.4:c.7033G= XP_005262212.2:p.Val2345=
XM_005262156.4:c.6985G= XP_005262213.2:p.Val2329=
XM_005262157.5:c.6946G= XP_005262214.2:p.Val2316=
XM_006724666.4:c.7033G= XP_006724729.1:p.Val2345=
XM_006724667.3:c.6871G= XP_006724730.1:p.Val2291=
XM_017029601.2:c.7060G= XP_016885090.1:p.Val2354=
XM_017029602.1:c.7030G= XP_016885091.1:p.Val2344=
XM_017029603.1:c.6982G= XP_016885092.1:p.Val2328=
XM_017029604.2:c.6949G= XP_016885093.1:p.Val2317=
XM_017029605.1:c.6946G= XP_016885094.1:p.Val2316=
XM_017029606.2:c.6919G= XP_016885095.1:p.Val2307=
XM_017029607.2:c.6916G= XP_016885096.1:p.Val2306=
XM_017029608.2:c.6868G= XP_016885097.1:p.Val2290=
XM_017029609.1:c.6832G= XP_016885098.1:p.Val2278=
XM_017029610.1:c.6829G= XP_016885099.1:p.Val2277=
XM_017029611.1:c.6784G= XP_016885100.1:p.Val2262=
XR_001755700.2:n.7449G=
NM_138270.4:c.7036G= NP_612114.2:p.Val2346=
NM_000489.6:c.7150G= MANE Select NP_000480.3:p.Val2384=
NM_138270.5:c.7036G= NP_612114.2:p.Val2346=