Canonical Allele Identifier: CA2438976965
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652330C= , CM000685.2:g.77652330C= GRCh38
NC_000023.10:g.76907820C= , CM000685.1:g.76907820C= GRCh37
NC_000023.9:g.76794476C= NCBI36
NG_008838.2:g.138892G=
NG_008838.3:g.138940G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4341G= MANE Select ENSP00000362441.4:p.Glu1447=
ENST00000373344.9:c.4341G= ENSP00000362441.4:p.Glu1447=
ENST00000395603.7:c.4227G= ENSP00000378967.3:p.Glu1409=
ENST00000480283.5:c.*3969G= ENSP00000480196.1:n.*3969G=
NM_000489.4:c.4341G= NP_000480.3:p.Glu1447=
NM_138270.3:c.4227G= NP_612114.2:p.Glu1409=
XM_005262153.3:c.4338G= XP_005262210.2:p.Glu1446=
XM_005262154.3:c.4254G= XP_005262211.2:p.Glu1418=
XM_005262155.3:c.4224G= XP_005262212.2:p.Glu1408=
XM_005262156.3:c.4176G= XP_005262213.2:p.Glu1392=
XM_005262157.3:c.4137G= XP_005262214.2:p.Glu1379=
XM_006724666.2:c.4224G= XP_006724729.1:p.Glu1408=
XM_006724667.2:c.4062G= XP_006724730.1:p.Glu1354=
XM_006724668.2:c.4341G= XP_006724731.1:p.Glu1447=
XR_938400.1:n.4609G=
NM_000489.5:c.4341G= NP_000480.3:p.Glu1447=
XM_005262153.5:c.4338G= XP_005262210.2:p.Glu1446=
XM_005262154.5:c.4254G= XP_005262211.2:p.Glu1418=
XM_005262155.4:c.4224G= XP_005262212.2:p.Glu1408=
XM_005262156.4:c.4176G= XP_005262213.2:p.Glu1392=
XM_005262157.5:c.4137G= XP_005262214.2:p.Glu1379=
XM_006724666.4:c.4224G= XP_006724729.1:p.Glu1408=
XM_006724667.3:c.4062G= XP_006724730.1:p.Glu1354=
XM_006724668.3:c.4341G= XP_006724731.1:p.Glu1447=
XM_017029601.2:c.4251G= XP_016885090.1:p.Glu1417=
XM_017029602.1:c.4221G= XP_016885091.1:p.Glu1407=
XM_017029603.1:c.4173G= XP_016885092.1:p.Glu1391=
XM_017029604.2:c.4140G= XP_016885093.1:p.Glu1380=
XM_017029605.1:c.4137G= XP_016885094.1:p.Glu1379=
XM_017029606.2:c.4110G= XP_016885095.1:p.Glu1370=
XM_017029607.2:c.4107G= XP_016885096.1:p.Glu1369=
XM_017029608.2:c.4059G= XP_016885097.1:p.Glu1353=
XM_017029609.1:c.4023G= XP_016885098.1:p.Glu1341=
XM_017029610.1:c.4020G= XP_016885099.1:p.Glu1340=
XM_017029611.1:c.3975G= XP_016885100.1:p.Glu1325=
XR_001755700.2:n.4566G=
NM_138270.4:c.4227G= NP_612114.2:p.Glu1409=
NM_000489.6:c.4341G= MANE Select NP_000480.3:p.Glu1447=
NM_138270.5:c.4227G= NP_612114.2:p.Glu1409=