Canonical Allele Identifier: CA2438976918
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652305C= , CM000685.2:g.77652305C= GRCh38
NC_000023.10:g.76907795C= , CM000685.1:g.76907795C= GRCh37
NC_000023.9:g.76794451C= NCBI36
NG_008838.2:g.138917G=
NG_008838.3:g.138965G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4366G= MANE Select ENSP00000362441.4:p.Glu1456=
ENST00000373344.9:c.4366G= ENSP00000362441.4:p.Glu1456=
ENST00000395603.7:c.4252G= ENSP00000378967.3:p.Glu1418=
ENST00000480283.5:c.*3994G= ENSP00000480196.1:n.*3994G=
NM_000489.4:c.4366G= NP_000480.3:p.Glu1456=
NM_138270.3:c.4252G= NP_612114.2:p.Glu1418=
XM_005262153.3:c.4363G= XP_005262210.2:p.Glu1455=
XM_005262154.3:c.4279G= XP_005262211.2:p.Glu1427=
XM_005262155.3:c.4249G= XP_005262212.2:p.Glu1417=
XM_005262156.3:c.4201G= XP_005262213.2:p.Glu1401=
XM_005262157.3:c.4162G= XP_005262214.2:p.Glu1388=
XM_006724666.2:c.4249G= XP_006724729.1:p.Glu1417=
XM_006724667.2:c.4087G= XP_006724730.1:p.Glu1363=
XM_006724668.2:c.4366G= XP_006724731.1:p.Glu1456=
XR_938400.1:n.4634G=
NM_000489.5:c.4366G= NP_000480.3:p.Glu1456=
XM_005262153.5:c.4363G= XP_005262210.2:p.Glu1455=
XM_005262154.5:c.4279G= XP_005262211.2:p.Glu1427=
XM_005262155.4:c.4249G= XP_005262212.2:p.Glu1417=
XM_005262156.4:c.4201G= XP_005262213.2:p.Glu1401=
XM_005262157.5:c.4162G= XP_005262214.2:p.Glu1388=
XM_006724666.4:c.4249G= XP_006724729.1:p.Glu1417=
XM_006724667.3:c.4087G= XP_006724730.1:p.Glu1363=
XM_006724668.3:c.4366G= XP_006724731.1:p.Glu1456=
XM_017029601.2:c.4276G= XP_016885090.1:p.Glu1426=
XM_017029602.1:c.4246G= XP_016885091.1:p.Glu1416=
XM_017029603.1:c.4198G= XP_016885092.1:p.Glu1400=
XM_017029604.2:c.4165G= XP_016885093.1:p.Glu1389=
XM_017029605.1:c.4162G= XP_016885094.1:p.Glu1388=
XM_017029606.2:c.4135G= XP_016885095.1:p.Glu1379=
XM_017029607.2:c.4132G= XP_016885096.1:p.Glu1378=
XM_017029608.2:c.4084G= XP_016885097.1:p.Glu1362=
XM_017029609.1:c.4048G= XP_016885098.1:p.Glu1350=
XM_017029610.1:c.4045G= XP_016885099.1:p.Glu1349=
XM_017029611.1:c.4000G= XP_016885100.1:p.Glu1334=
XR_001755700.2:n.4591G=
NM_138270.4:c.4252G= NP_612114.2:p.Glu1418=
NM_000489.6:c.4366G= MANE Select NP_000480.3:p.Glu1456=
NM_138270.5:c.4252G= NP_612114.2:p.Glu1418=