Canonical Allele Identifier: CA2438976848
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652276A= , CM000685.2:g.77652276A= GRCh38
NC_000023.10:g.76907766A= , CM000685.1:g.76907766A= GRCh37
NC_000023.9:g.76794422A= NCBI36
NG_008838.2:g.138946T=
NG_008838.3:g.138994T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4395T= MANE Select ENSP00000362441.4:p.Asp1465=
ENST00000373344.9:c.4395T= ENSP00000362441.4:p.Asp1465=
ENST00000395603.7:c.4281T= ENSP00000378967.3:p.Asp1427=
ENST00000480283.5:c.*4023T= ENSP00000480196.1:n.*4023T=
ENST00000623242.3:c.1T=
NM_000489.4:c.4395T= NP_000480.3:p.Asp1465=
NM_138270.3:c.4281T= NP_612114.2:p.Asp1427=
XM_005262153.3:c.4392T= XP_005262210.2:p.Asp1464=
XM_005262154.3:c.4308T= XP_005262211.2:p.Asp1436=
XM_005262155.3:c.4278T= XP_005262212.2:p.Asp1426=
XM_005262156.3:c.4230T= XP_005262213.2:p.Asp1410=
XM_005262157.3:c.4191T= XP_005262214.2:p.Asp1397=
XM_006724666.2:c.4278T= XP_006724729.1:p.Asp1426=
XM_006724667.2:c.4116T= XP_006724730.1:p.Asp1372=
XM_006724668.2:c.4395T= XP_006724731.1:p.Asp1465=
XR_938400.1:n.4663T=
NM_000489.5:c.4395T= NP_000480.3:p.Asp1465=
XM_005262153.5:c.4392T= XP_005262210.2:p.Asp1464=
XM_005262154.5:c.4308T= XP_005262211.2:p.Asp1436=
XM_005262155.4:c.4278T= XP_005262212.2:p.Asp1426=
XM_005262156.4:c.4230T= XP_005262213.2:p.Asp1410=
XM_005262157.5:c.4191T= XP_005262214.2:p.Asp1397=
XM_006724666.4:c.4278T= XP_006724729.1:p.Asp1426=
XM_006724667.3:c.4116T= XP_006724730.1:p.Asp1372=
XM_006724668.3:c.4395T= XP_006724731.1:p.Asp1465=
XM_017029601.2:c.4305T= XP_016885090.1:p.Asp1435=
XM_017029602.1:c.4275T= XP_016885091.1:p.Asp1425=
XM_017029603.1:c.4227T= XP_016885092.1:p.Asp1409=
XM_017029604.2:c.4194T= XP_016885093.1:p.Asp1398=
XM_017029605.1:c.4191T= XP_016885094.1:p.Asp1397=
XM_017029606.2:c.4164T= XP_016885095.1:p.Asp1388=
XM_017029607.2:c.4161T= XP_016885096.1:p.Asp1387=
XM_017029608.2:c.4113T= XP_016885097.1:p.Asp1371=
XM_017029609.1:c.4077T= XP_016885098.1:p.Asp1359=
XM_017029610.1:c.4074T= XP_016885099.1:p.Asp1358=
XM_017029611.1:c.4029T= XP_016885100.1:p.Asp1343=
XR_001755700.2:n.4620T=
NM_138270.4:c.4281T= NP_612114.2:p.Asp1427=
NM_000489.6:c.4395T= MANE Select NP_000480.3:p.Asp1465=
NM_138270.5:c.4281T= NP_612114.2:p.Asp1427=