Canonical Allele Identifier: CA2438951403
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77574335T= , CM000685.2:g.77574335T= GRCh38
NC_000023.10:g.76829800T= , CM000685.1:g.76829800T= GRCh37
NC_000023.9:g.76716456T= NCBI36
NG_008838.2:g.216887A=
NG_008838.3:g.216935A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.6241A= MANE Select ENSP00000362441.4:p.Ile2081=
ENST00000636152.1:n.76A=
ENST00000675732.1:c.1339A= ENSP00000502598.1:p.Ile447=
ENST00000373344.9:c.6241A= ENSP00000362441.4:p.Ile2081=
ENST00000395603.7:c.6127A= ENSP00000378967.3:p.Ile2043=
ENST00000480283.5:c.*5869A= ENSP00000480196.1:n.*5869A=
ENST00000623316.1:c.725A=
ENST00000623706.3:n.3311A=
NM_000489.4:c.6241A= NP_000480.3:p.Ile2081=
NM_138270.3:c.6127A= NP_612114.2:p.Ile2043=
XM_005262153.3:c.6238A= XP_005262210.2:p.Ile2080=
XM_005262154.3:c.6154A= XP_005262211.2:p.Ile2052=
XM_005262155.3:c.6124A= XP_005262212.2:p.Ile2042=
XM_005262156.3:c.6076A= XP_005262213.2:p.Ile2026=
XM_005262157.3:c.6037A= XP_005262214.2:p.Ile2013=
XM_006724666.2:c.6124A= XP_006724729.1:p.Ile2042=
XM_006724667.2:c.5962A= XP_006724730.1:p.Ile1988=
XR_938400.1:n.6583A=
NM_000489.5:c.6241A= NP_000480.3:p.Ile2081=
XM_005262153.5:c.6238A= XP_005262210.2:p.Ile2080=
XM_005262154.5:c.6154A= XP_005262211.2:p.Ile2052=
XM_005262155.4:c.6124A= XP_005262212.2:p.Ile2042=
XM_005262156.4:c.6076A= XP_005262213.2:p.Ile2026=
XM_005262157.5:c.6037A= XP_005262214.2:p.Ile2013=
XM_006724666.4:c.6124A= XP_006724729.1:p.Ile2042=
XM_006724667.3:c.5962A= XP_006724730.1:p.Ile1988=
XM_017029601.2:c.6151A= XP_016885090.1:p.Ile2051=
XM_017029602.1:c.6121A= XP_016885091.1:p.Ile2041=
XM_017029603.1:c.6073A= XP_016885092.1:p.Ile2025=
XM_017029604.2:c.6040A= XP_016885093.1:p.Ile2014=
XM_017029605.1:c.6037A= XP_016885094.1:p.Ile2013=
XM_017029606.2:c.6010A= XP_016885095.1:p.Ile2004=
XM_017029607.2:c.6007A= XP_016885096.1:p.Ile2003=
XM_017029608.2:c.5959A= XP_016885097.1:p.Ile1987=
XM_017029609.1:c.5923A= XP_016885098.1:p.Ile1975=
XM_017029610.1:c.5920A= XP_016885099.1:p.Ile1974=
XM_017029611.1:c.5875A= XP_016885100.1:p.Ile1959=
XR_001755700.2:n.6540A=
NM_138270.4:c.6127A= NP_612114.2:p.Ile2043=
NM_000489.6:c.6241A= MANE Select NP_000480.3:p.Ile2081=
NM_138270.5:c.6127A= NP_612114.2:p.Ile2043=