Canonical Allele Identifier: CA2694140407
Gene: ATRX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77574464_77574465del , CM000685.2:g.77574464_77574465del GRCh38
NC_000023.10:g.76829929_76829930del , CM000685.1:g.76829929_76829930del GRCh37
NC_000023.9:g.76716585_76716586del NCBI36
NG_008838.2:g.216764_216765del
NG_008838.3:g.216812_216813del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.6218-100_6218-99del MANE Select ENSP00000362441.4:n.6218-100_6218-99del
ENST00000636152.1:n.53-100_53-99del
ENST00000675732.1:c.1316-100_1316-99del ENSP00000502598.1:n.1316-100_1316-99del
ENST00000373344.9:c.6218-100_6218-99del ENSP00000362441.4:n.6218-100_6218-99del
ENST00000395603.7:c.6104-100_6104-99del ENSP00000378967.3:n.6104-100_6104-99del
ENST00000480283.5:c.*5846-100_*5846-99del ENSP00000480196.1:n.*5846-100_*5846-99del
ENST00000623316.1:c.702-100_702-99del
ENST00000623706.3:n.3288-100_3288-99del
NM_000489.4:c.6218-100_6218-99del NP_000480.3:n.6218-100_6218-99del
NM_138270.3:c.6104-100_6104-99del NP_612114.2:n.6104-100_6104-99del
XM_005262153.3:c.6215-100_6215-99del XP_005262210.2:n.6215-100_6215-99del
XM_005262154.3:c.6131-100_6131-99del XP_005262211.2:n.6131-100_6131-99del
XM_005262155.3:c.6101-100_6101-99del XP_005262212.2:n.6101-100_6101-99del
XM_005262156.3:c.6053-100_6053-99del XP_005262213.2:n.6053-100_6053-99del
XM_005262157.3:c.6014-100_6014-99del XP_005262214.2:n.6014-100_6014-99del
XM_006724666.2:c.6101-100_6101-99del XP_006724729.1:n.6101-100_6101-99del
XM_006724667.2:c.5939-100_5939-99del XP_006724730.1:n.5939-100_5939-99del
XR_938400.1:n.6560-100_6560-99del
NM_000489.5:c.6218-100_6218-99del NP_000480.3:n.6218-100_6218-99del
XM_005262153.5:c.6215-100_6215-99del XP_005262210.2:n.6215-100_6215-99del
XM_005262154.5:c.6131-100_6131-99del XP_005262211.2:n.6131-100_6131-99del
XM_005262155.4:c.6101-100_6101-99del XP_005262212.2:n.6101-100_6101-99del
XM_005262156.4:c.6053-100_6053-99del XP_005262213.2:n.6053-100_6053-99del
XM_005262157.5:c.6014-100_6014-99del XP_005262214.2:n.6014-100_6014-99del
XM_006724666.4:c.6101-100_6101-99del XP_006724729.1:n.6101-100_6101-99del
XM_006724667.3:c.5939-100_5939-99del XP_006724730.1:n.5939-100_5939-99del
XM_017029601.2:c.6128-100_6128-99del XP_016885090.1:n.6128-100_6128-99del
XM_017029602.1:c.6098-100_6098-99del XP_016885091.1:n.6098-100_6098-99del
XM_017029603.1:c.6050-100_6050-99del XP_016885092.1:n.6050-100_6050-99del
XM_017029604.2:c.6017-100_6017-99del XP_016885093.1:n.6017-100_6017-99del
XM_017029605.1:c.6014-100_6014-99del XP_016885094.1:n.6014-100_6014-99del
XM_017029606.2:c.5987-100_5987-99del XP_016885095.1:n.5987-100_5987-99del
XM_017029607.2:c.5984-100_5984-99del XP_016885096.1:n.5984-100_5984-99del
XM_017029608.2:c.5936-100_5936-99del XP_016885097.1:n.5936-100_5936-99del
XM_017029609.1:c.5900-100_5900-99del XP_016885098.1:n.5900-100_5900-99del
XM_017029610.1:c.5897-100_5897-99del XP_016885099.1:n.5897-100_5897-99del
XM_017029611.1:c.5852-100_5852-99del XP_016885100.1:n.5852-100_5852-99del
XR_001755700.2:n.6517-100_6517-99del
NM_138270.4:c.6104-100_6104-99del NP_612114.2:n.6104-100_6104-99del
NM_000489.6:c.6218-100_6218-99del MANE Select NP_000480.3:n.6218-100_6218-99del
NM_138270.5:c.6104-100_6104-99del NP_612114.2:n.6104-100_6104-99del