Canonical Allele Identifier: CA2438976959
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652326T= , CM000685.2:g.77652326T= GRCh38
NC_000023.10:g.76907816T= , CM000685.1:g.76907816T= GRCh37
NC_000023.9:g.76794472T= NCBI36
NG_008838.2:g.138896A=
NG_008838.3:g.138944A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4345A= MANE Select ENSP00000362441.4:p.Lys1449=
ENST00000373344.9:c.4345A= ENSP00000362441.4:p.Lys1449=
ENST00000395603.7:c.4231A= ENSP00000378967.3:p.Lys1411=
ENST00000480283.5:c.*3973A= ENSP00000480196.1:n.*3973A=
NM_000489.4:c.4345A= NP_000480.3:p.Lys1449=
NM_138270.3:c.4231A= NP_612114.2:p.Lys1411=
XM_005262153.3:c.4342A= XP_005262210.2:p.Lys1448=
XM_005262154.3:c.4258A= XP_005262211.2:p.Lys1420=
XM_005262155.3:c.4228A= XP_005262212.2:p.Lys1410=
XM_005262156.3:c.4180A= XP_005262213.2:p.Lys1394=
XM_005262157.3:c.4141A= XP_005262214.2:p.Lys1381=
XM_006724666.2:c.4228A= XP_006724729.1:p.Lys1410=
XM_006724667.2:c.4066A= XP_006724730.1:p.Lys1356=
XM_006724668.2:c.4345A= XP_006724731.1:p.Lys1449=
XR_938400.1:n.4613A=
NM_000489.5:c.4345A= NP_000480.3:p.Lys1449=
XM_005262153.5:c.4342A= XP_005262210.2:p.Lys1448=
XM_005262154.5:c.4258A= XP_005262211.2:p.Lys1420=
XM_005262155.4:c.4228A= XP_005262212.2:p.Lys1410=
XM_005262156.4:c.4180A= XP_005262213.2:p.Lys1394=
XM_005262157.5:c.4141A= XP_005262214.2:p.Lys1381=
XM_006724666.4:c.4228A= XP_006724729.1:p.Lys1410=
XM_006724667.3:c.4066A= XP_006724730.1:p.Lys1356=
XM_006724668.3:c.4345A= XP_006724731.1:p.Lys1449=
XM_017029601.2:c.4255A= XP_016885090.1:p.Lys1419=
XM_017029602.1:c.4225A= XP_016885091.1:p.Lys1409=
XM_017029603.1:c.4177A= XP_016885092.1:p.Lys1393=
XM_017029604.2:c.4144A= XP_016885093.1:p.Lys1382=
XM_017029605.1:c.4141A= XP_016885094.1:p.Lys1381=
XM_017029606.2:c.4114A= XP_016885095.1:p.Lys1372=
XM_017029607.2:c.4111A= XP_016885096.1:p.Lys1371=
XM_017029608.2:c.4063A= XP_016885097.1:p.Lys1355=
XM_017029609.1:c.4027A= XP_016885098.1:p.Lys1343=
XM_017029610.1:c.4024A= XP_016885099.1:p.Lys1342=
XM_017029611.1:c.3979A= XP_016885100.1:p.Lys1327=
XR_001755700.2:n.4570A=
NM_138270.4:c.4231A= NP_612114.2:p.Lys1411=
NM_000489.6:c.4345A= MANE Select NP_000480.3:p.Lys1449=
NM_138270.5:c.4231A= NP_612114.2:p.Lys1411=