Canonical Allele Identifier: CA2438976864
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652282C= , CM000685.2:g.77652282C= GRCh38
NC_000023.10:g.76907772C= , CM000685.1:g.76907772C= GRCh37
NC_000023.9:g.76794428C= NCBI36
NG_008838.2:g.138940G=
NG_008838.3:g.138988G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4389G= MANE Select ENSP00000362441.4:p.Glu1463=
ENST00000373344.9:c.4389G= ENSP00000362441.4:p.Glu1463=
ENST00000395603.7:c.4275G= ENSP00000378967.3:p.Glu1425=
ENST00000480283.5:c.*4017G= ENSP00000480196.1:n.*4017G=
NM_000489.4:c.4389G= NP_000480.3:p.Glu1463=
NM_138270.3:c.4275G= NP_612114.2:p.Glu1425=
XM_005262153.3:c.4386G= XP_005262210.2:p.Glu1462=
XM_005262154.3:c.4302G= XP_005262211.2:p.Glu1434=
XM_005262155.3:c.4272G= XP_005262212.2:p.Glu1424=
XM_005262156.3:c.4224G= XP_005262213.2:p.Glu1408=
XM_005262157.3:c.4185G= XP_005262214.2:p.Glu1395=
XM_006724666.2:c.4272G= XP_006724729.1:p.Glu1424=
XM_006724667.2:c.4110G= XP_006724730.1:p.Glu1370=
XM_006724668.2:c.4389G= XP_006724731.1:p.Glu1463=
XR_938400.1:n.4657G=
NM_000489.5:c.4389G= NP_000480.3:p.Glu1463=
XM_005262153.5:c.4386G= XP_005262210.2:p.Glu1462=
XM_005262154.5:c.4302G= XP_005262211.2:p.Glu1434=
XM_005262155.4:c.4272G= XP_005262212.2:p.Glu1424=
XM_005262156.4:c.4224G= XP_005262213.2:p.Glu1408=
XM_005262157.5:c.4185G= XP_005262214.2:p.Glu1395=
XM_006724666.4:c.4272G= XP_006724729.1:p.Glu1424=
XM_006724667.3:c.4110G= XP_006724730.1:p.Glu1370=
XM_006724668.3:c.4389G= XP_006724731.1:p.Glu1463=
XM_017029601.2:c.4299G= XP_016885090.1:p.Glu1433=
XM_017029602.1:c.4269G= XP_016885091.1:p.Glu1423=
XM_017029603.1:c.4221G= XP_016885092.1:p.Glu1407=
XM_017029604.2:c.4188G= XP_016885093.1:p.Glu1396=
XM_017029605.1:c.4185G= XP_016885094.1:p.Glu1395=
XM_017029606.2:c.4158G= XP_016885095.1:p.Glu1386=
XM_017029607.2:c.4155G= XP_016885096.1:p.Glu1385=
XM_017029608.2:c.4107G= XP_016885097.1:p.Glu1369=
XM_017029609.1:c.4071G= XP_016885098.1:p.Glu1357=
XM_017029610.1:c.4068G= XP_016885099.1:p.Glu1356=
XM_017029611.1:c.4023G= XP_016885100.1:p.Glu1341=
XR_001755700.2:n.4614G=
NM_138270.4:c.4275G= NP_612114.2:p.Glu1425=
NM_000489.6:c.4389G= MANE Select NP_000480.3:p.Glu1463=
NM_138270.5:c.4275G= NP_612114.2:p.Glu1425=