Canonical Allele Identifier: CA2438989300
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77688755G= , CM000685.2:g.77688755G= GRCh38
NC_000023.10:g.76944248G= , CM000685.1:g.76944248G= GRCh37
NC_000023.9:g.76830904G= NCBI36
NG_008838.2:g.102467C=
NG_008838.3:g.102515C=

Transcript Alleles

HGVS Amino-acid change
ENST00000373344.11:c.594+63C= MANE Select ENSP00000362441.4:n.594+63C=
ENST00000373344.9:c.594+63C= ENSP00000362441.4:n.594+63C=
ENST00000395603.7:c.480+63C= ENSP00000378967.3:n.480+63C=
ENST00000480283.5:c.*222+63C= ENSP00000480196.1:n.*222+63C=
ENST00000623321.3:c.429+63C= ENSP00000485127.1:n.429+63C=
ENST00000624032.3:c.594+63C= ENSP00000485253.1:n.594+63C=
ENST00000624166.3:c.477+63C= ENSP00000485103.1:n.477+63C=
ENST00000624668.3:c.315+63C= ENSP00000485100.1:n.315+63C=
ENST00000625063.3:c.409+63C=
NM_000489.4:c.594+63C= NP_000480.3:n.594+63C=
NM_138270.3:c.480+63C= NP_612114.2:n.480+63C=
XM_005262153.3:c.591+63C= XP_005262210.2:n.591+63C=
XM_005262154.3:c.594+63C= XP_005262211.2:n.594+63C=
XM_005262155.3:c.477+63C= XP_005262212.2:n.477+63C=
XM_005262156.3:c.429+63C= XP_005262213.2:n.429+63C=
XM_005262157.3:c.477+63C= XP_005262214.2:n.477+63C=
XM_006724666.2:c.477+63C= XP_006724729.1:n.477+63C=
XM_006724667.2:c.315+63C= XP_006724730.1:n.315+63C=
XM_006724668.2:c.594+63C= XP_006724731.1:n.594+63C=
XR_938400.1:n.862+63C=
NM_000489.5:c.594+63C= NP_000480.3:n.594+63C=
XM_005262153.5:c.591+63C= XP_005262210.2:n.591+63C=
XM_005262154.5:c.594+63C= XP_005262211.2:n.594+63C=
XM_005262155.4:c.477+63C= XP_005262212.2:n.477+63C=
XM_005262156.4:c.429+63C= XP_005262213.2:n.429+63C=
XM_005262157.5:c.477+63C= XP_005262214.2:n.477+63C=
XM_006724666.4:c.477+63C= XP_006724729.1:n.477+63C=
XM_006724667.3:c.315+63C= XP_006724730.1:n.315+63C=
XM_006724668.3:c.594+63C= XP_006724731.1:n.594+63C=
XM_017029601.2:c.591+63C= XP_016885090.1:n.591+63C=
XM_017029602.1:c.474+63C= XP_016885091.1:n.474+63C=
XM_017029603.1:c.426+63C= XP_016885092.1:n.426+63C=
XM_017029604.2:c.480+63C= XP_016885093.1:n.480+63C=
XM_017029605.1:c.477+63C= XP_016885094.1:n.477+63C=
XM_017029606.2:c.363+63C= XP_016885095.1:n.363+63C=
XM_017029607.2:c.360+63C= XP_016885096.1:n.360+63C=
XM_017029608.2:c.312+63C= XP_016885097.1:n.312+63C=
XM_017029609.1:c.363+63C= XP_016885098.1:n.363+63C=
XM_017029610.1:c.360+63C= XP_016885099.1:n.360+63C=
XM_017029611.1:c.315+63C= XP_016885100.1:n.315+63C=
XR_001755700.2:n.819+63C=
NM_138270.4:c.480+63C= NP_612114.2:n.480+63C=
NM_000489.6:c.594+63C= MANE Select NP_000480.3:n.594+63C=
NM_138270.5:c.480+63C= NP_612114.2:n.480+63C=