Canonical Allele Identifier: CA2438956384
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77589810_77589812delinsGAC , CM000685.2:g.77589810_77589812delinsGAC GRCh38
NC_000023.10:g.76845280_76845282delinsGAC , CM000685.1:g.76845280_76845282delinsGAC GRCh37
NC_000023.9:g.76731936_76731938delinsGAC NCBI36
NG_008838.2:g.201410_201412delinsGTC
NG_008838.3:g.201458_201460delinsGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.6217+22_6217+24delinsGTC MANE Select ENSP00000362441.4:n.6217+22_6217+24delinsGTC
ENST00000636868.1:n.39+22_39+24delinsGTC
ENST00000675732.1:c.1315+22_1315+24delinsGTC ENSP00000502598.1:n.1315+22_1315+24delinsGTC
ENST00000373344.9:c.6217+22_6217+24delinsGTC ENSP00000362441.4:n.6217+22_6217+24delinsGTC
ENST00000395603.7:c.6103+22_6103+24delinsGTC ENSP00000378967.3:n.6103+22_6103+24delinsGTC
ENST00000480283.5:c.*5845+22_*5845+24delinsGTC ENSP00000480196.1:n.*5845+22_*5845+24delinsGTC
ENST00000623316.1:c.701+22_701+24delinsGTC
ENST00000623706.3:n.3287+22_3287+24delinsGTC
NM_000489.4:c.6217+22_6217+24delinsGTC NP_000480.3:n.6217+22_6217+24delinsGTC
NM_138270.3:c.6103+22_6103+24delinsGTC NP_612114.2:n.6103+22_6103+24delinsGTC
XM_005262153.3:c.6214+22_6214+24delinsGTC XP_005262210.2:n.6214+22_6214+24delinsGTC
XM_005262154.3:c.6130+22_6130+24delinsGTC XP_005262211.2:n.6130+22_6130+24delinsGTC
XM_005262155.3:c.6100+22_6100+24delinsGTC XP_005262212.2:n.6100+22_6100+24delinsGTC
XM_005262156.3:c.6052+22_6052+24delinsGTC XP_005262213.2:n.6052+22_6052+24delinsGTC
XM_005262157.3:c.6013+22_6013+24delinsGTC XP_005262214.2:n.6013+22_6013+24delinsGTC
XM_006724666.2:c.6100+22_6100+24delinsGTC XP_006724729.1:n.6100+22_6100+24delinsGTC
XM_006724667.2:c.5938+22_5938+24delinsGTC XP_006724730.1:n.5938+22_5938+24delinsGTC
XR_938400.1:n.6559+22_6559+24delinsGTC
NM_000489.5:c.6217+22_6217+24delinsGTC NP_000480.3:n.6217+22_6217+24delinsGTC
XM_005262153.5:c.6214+22_6214+24delinsGTC XP_005262210.2:n.6214+22_6214+24delinsGTC
XM_005262154.5:c.6130+22_6130+24delinsGTC XP_005262211.2:n.6130+22_6130+24delinsGTC
XM_005262155.4:c.6100+22_6100+24delinsGTC XP_005262212.2:n.6100+22_6100+24delinsGTC
XM_005262156.4:c.6052+22_6052+24delinsGTC XP_005262213.2:n.6052+22_6052+24delinsGTC
XM_005262157.5:c.6013+22_6013+24delinsGTC XP_005262214.2:n.6013+22_6013+24delinsGTC
XM_006724666.4:c.6100+22_6100+24delinsGTC XP_006724729.1:n.6100+22_6100+24delinsGTC
XM_006724667.3:c.5938+22_5938+24delinsGTC XP_006724730.1:n.5938+22_5938+24delinsGTC
XM_017029601.2:c.6127+22_6127+24delinsGTC XP_016885090.1:n.6127+22_6127+24delinsGTC
XM_017029602.1:c.6097+22_6097+24delinsGTC XP_016885091.1:n.6097+22_6097+24delinsGTC
XM_017029603.1:c.6049+22_6049+24delinsGTC XP_016885092.1:n.6049+22_6049+24delinsGTC
XM_017029604.2:c.6016+22_6016+24delinsGTC XP_016885093.1:n.6016+22_6016+24delinsGTC
XM_017029605.1:c.6013+22_6013+24delinsGTC XP_016885094.1:n.6013+22_6013+24delinsGTC
XM_017029606.2:c.5986+22_5986+24delinsGTC XP_016885095.1:n.5986+22_5986+24delinsGTC
XM_017029607.2:c.5983+22_5983+24delinsGTC XP_016885096.1:n.5983+22_5983+24delinsGTC
XM_017029608.2:c.5935+22_5935+24delinsGTC XP_016885097.1:n.5935+22_5935+24delinsGTC
XM_017029609.1:c.5899+22_5899+24delinsGTC XP_016885098.1:n.5899+22_5899+24delinsGTC
XM_017029610.1:c.5896+22_5896+24delinsGTC XP_016885099.1:n.5896+22_5896+24delinsGTC
XM_017029611.1:c.5851+22_5851+24delinsGTC XP_016885100.1:n.5851+22_5851+24delinsGTC
XR_001755700.2:n.6516+22_6516+24delinsGTC
NM_138270.4:c.6103+22_6103+24delinsGTC NP_612114.2:n.6103+22_6103+24delinsGTC
NM_000489.6:c.6217+22_6217+24delinsGTC MANE Select NP_000480.3:n.6217+22_6217+24delinsGTC
NM_138270.5:c.6103+22_6103+24delinsGTC NP_612114.2:n.6103+22_6103+24delinsGTC