Canonical Allele Identifier: CA2438933060
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77520826C= , CM000685.2:g.77520826C= GRCh38
NC_000023.10:g.76776304C= , CM000685.1:g.76776304C= GRCh37
NC_000023.9:g.76662960C= NCBI36
NG_008838.2:g.270396G=
NG_008838.3:g.270444G=

Transcript Alleles

HGVS Amino-acid change
ENST00000373344.11:c.7162G= MANE Select ENSP00000362441.4:p.Glu2388=
ENST00000675732.1:c.2260G= ENSP00000502598.1:p.Glu754=
ENST00000373344.9:c.7162G= ENSP00000362441.4:p.Glu2388=
ENST00000395603.7:c.7048G= ENSP00000378967.3:p.Glu2350=
ENST00000480283.5:c.*6790G= ENSP00000480196.1:n.*6790G=
ENST00000623706.3:n.5482G=
ENST00000624766.1:n.393G=
NM_000489.4:c.7162G= NP_000480.3:p.Glu2388=
NM_138270.3:c.7048G= NP_612114.2:p.Glu2350=
XM_005262153.3:c.7159G= XP_005262210.2:p.Glu2387=
XM_005262154.3:c.7075G= XP_005262211.2:p.Glu2359=
XM_005262155.3:c.7045G= XP_005262212.2:p.Glu2349=
XM_005262156.3:c.6997G= XP_005262213.2:p.Glu2333=
XM_005262157.3:c.6958G= XP_005262214.2:p.Glu2320=
XM_006724666.2:c.7045G= XP_006724729.1:p.Glu2349=
XM_006724667.2:c.6883G= XP_006724730.1:p.Glu2295=
XR_938400.1:n.8754G=
NM_000489.5:c.7162G= NP_000480.3:p.Glu2388=
XM_005262153.5:c.7159G= XP_005262210.2:p.Glu2387=
XM_005262154.5:c.7075G= XP_005262211.2:p.Glu2359=
XM_005262155.4:c.7045G= XP_005262212.2:p.Glu2349=
XM_005262156.4:c.6997G= XP_005262213.2:p.Glu2333=
XM_005262157.5:c.6958G= XP_005262214.2:p.Glu2320=
XM_006724666.4:c.7045G= XP_006724729.1:p.Glu2349=
XM_006724667.3:c.6883G= XP_006724730.1:p.Glu2295=
XM_017029601.2:c.7072G= XP_016885090.1:p.Glu2358=
XM_017029602.1:c.7042G= XP_016885091.1:p.Glu2348=
XM_017029603.1:c.6994G= XP_016885092.1:p.Glu2332=
XM_017029604.2:c.6961G= XP_016885093.1:p.Glu2321=
XM_017029605.1:c.6958G= XP_016885094.1:p.Glu2320=
XM_017029606.2:c.6931G= XP_016885095.1:p.Glu2311=
XM_017029607.2:c.6928G= XP_016885096.1:p.Glu2310=
XM_017029608.2:c.6880G= XP_016885097.1:p.Glu2294=
XM_017029609.1:c.6844G= XP_016885098.1:p.Glu2282=
XM_017029610.1:c.6841G= XP_016885099.1:p.Glu2281=
XM_017029611.1:c.6796G= XP_016885100.1:p.Glu2266=
XR_001755700.2:n.7461G=
NM_138270.4:c.7048G= NP_612114.2:p.Glu2350=
NM_000489.6:c.7162G= MANE Select NP_000480.3:p.Glu2388=
NM_138270.5:c.7048G= NP_612114.2:p.Glu2350=