Canonical Allele Identifier: CA2438929017
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508363C= , CM000685.2:g.77508363C= GRCh38
NC_000023.10:g.76763841C= , CM000685.1:g.76763841C= GRCh37
NC_000023.9:g.76650497C= NCBI36
NG_008838.2:g.282859G=
NG_008838.3:g.282907G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7467G= MANE Select ENSP00000362441.4:p.Gly2489=
ENST00000675732.1:c.2565G= ENSP00000502598.1:p.Gly855=
ENST00000373344.9:c.7467G= ENSP00000362441.4:p.Gly2489=
ENST00000395603.7:c.7353G= ENSP00000378967.3:p.Gly2451=
ENST00000480283.5:c.*7095G= ENSP00000480196.1:n.*7095G=
ENST00000623706.3:n.5787G=
NM_000489.4:c.7467G= NP_000480.3:p.Gly2489=
NM_138270.3:c.7353G= NP_612114.2:p.Gly2451=
XM_005262153.3:c.7464G= XP_005262210.2:p.Gly2488=
XM_005262154.3:c.7380G= XP_005262211.2:p.Gly2460=
XM_005262155.3:c.7350G= XP_005262212.2:p.Gly2450=
XM_005262156.3:c.7302G= XP_005262213.2:p.Gly2434=
XM_005262157.3:c.7263G= XP_005262214.2:p.Gly2421=
XM_006724666.2:c.7350G= XP_006724729.1:p.Gly2450=
XM_006724667.2:c.7188G= XP_006724730.1:p.Gly2396=
XR_938400.1:n.9059G=
NM_000489.5:c.7467G= NP_000480.3:p.Gly2489=
XM_005262153.5:c.7464G= XP_005262210.2:p.Gly2488=
XM_005262154.5:c.7380G= XP_005262211.2:p.Gly2460=
XM_005262155.4:c.7350G= XP_005262212.2:p.Gly2450=
XM_005262156.4:c.7302G= XP_005262213.2:p.Gly2434=
XM_005262157.5:c.7263G= XP_005262214.2:p.Gly2421=
XM_006724666.4:c.7350G= XP_006724729.1:p.Gly2450=
XM_006724667.3:c.7188G= XP_006724730.1:p.Gly2396=
XM_017029601.2:c.7377G= XP_016885090.1:p.Gly2459=
XM_017029602.1:c.7347G= XP_016885091.1:p.Gly2449=
XM_017029603.1:c.7299G= XP_016885092.1:p.Gly2433=
XM_017029604.2:c.7266G= XP_016885093.1:p.Gly2422=
XM_017029605.1:c.7263G= XP_016885094.1:p.Gly2421=
XM_017029606.2:c.7236G= XP_016885095.1:p.Gly2412=
XM_017029607.2:c.7233G= XP_016885096.1:p.Gly2411=
XM_017029608.2:c.7185G= XP_016885097.1:p.Gly2395=
XM_017029609.1:c.7149G= XP_016885098.1:p.Gly2383=
XM_017029610.1:c.7146G= XP_016885099.1:p.Gly2382=
XM_017029611.1:c.7101G= XP_016885100.1:p.Gly2367=
XR_001755700.2:n.7766G=
NM_138270.4:c.7353G= NP_612114.2:p.Gly2451=
NM_000489.6:c.7467G= MANE Select NP_000480.3:p.Gly2489=
NM_138270.5:c.7353G= NP_612114.2:p.Gly2451=