Canonical Allele Identifier: CA2551077118
Gene: ATRX HGNC NCBI

Linked Data

dbSNP Id: rs2148020194

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77574370_77574371insTGATGAAA , CM000685.2:g.77574370_77574371insTGATGAAA GRCh38
NC_000023.10:g.76829835_76829836insTGATGAAA , CM000685.1:g.76829835_76829836insTGATGAAA GRCh37
NC_000023.9:g.76716491_76716492insTGATGAAA NCBI36
NG_008838.2:g.216853_216854insTCATCATT
NG_008838.3:g.216901_216902insTCATCATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.6218-11_6218-10insTCATCATT MANE Select ENSP00000362441.4:n.6218-11_6218-10insTCATCATT
ENST00000636152.1:n.53-11_53-10insTCATCATT
ENST00000675732.1:c.1316-11_1316-10insTCATCATT ENSP00000502598.1:n.1316-11_1316-10insTCATCATT
ENST00000373344.9:c.6218-11_6218-10insTCATCATT ENSP00000362441.4:n.6218-11_6218-10insTCATCATT
ENST00000395603.7:c.6104-11_6104-10insTCATCATT ENSP00000378967.3:n.6104-11_6104-10insTCATCATT
ENST00000480283.5:c.*5846-11_*5846-10insTCATCATT ENSP00000480196.1:n.*5846-11_*5846-10insTCATCATT
ENST00000623316.1:c.702-11_702-10insTCATCATT
ENST00000623706.3:n.3288-11_3288-10insTCATCATT
NM_000489.4:c.6218-11_6218-10insTCATCATT NP_000480.3:n.6218-11_6218-10insTCATCATT
NM_138270.3:c.6104-11_6104-10insTCATCATT NP_612114.2:n.6104-11_6104-10insTCATCATT
XM_005262153.3:c.6215-11_6215-10insTCATCATT XP_005262210.2:n.6215-11_6215-10insTCATCATT
XM_005262154.3:c.6131-11_6131-10insTCATCATT XP_005262211.2:n.6131-11_6131-10insTCATCATT
XM_005262155.3:c.6101-11_6101-10insTCATCATT XP_005262212.2:n.6101-11_6101-10insTCATCATT
XM_005262156.3:c.6053-11_6053-10insTCATCATT XP_005262213.2:n.6053-11_6053-10insTCATCATT
XM_005262157.3:c.6014-11_6014-10insTCATCATT XP_005262214.2:n.6014-11_6014-10insTCATCATT
XM_006724666.2:c.6101-11_6101-10insTCATCATT XP_006724729.1:n.6101-11_6101-10insTCATCATT
XM_006724667.2:c.5939-11_5939-10insTCATCATT XP_006724730.1:n.5939-11_5939-10insTCATCATT
XR_938400.1:n.6560-11_6560-10insTCATCATT
NM_000489.5:c.6218-11_6218-10insTCATCATT NP_000480.3:n.6218-11_6218-10insTCATCATT
XM_005262153.5:c.6215-11_6215-10insTCATCATT XP_005262210.2:n.6215-11_6215-10insTCATCATT
XM_005262154.5:c.6131-11_6131-10insTCATCATT XP_005262211.2:n.6131-11_6131-10insTCATCATT
XM_005262155.4:c.6101-11_6101-10insTCATCATT XP_005262212.2:n.6101-11_6101-10insTCATCATT
XM_005262156.4:c.6053-11_6053-10insTCATCATT XP_005262213.2:n.6053-11_6053-10insTCATCATT
XM_005262157.5:c.6014-11_6014-10insTCATCATT XP_005262214.2:n.6014-11_6014-10insTCATCATT
XM_006724666.4:c.6101-11_6101-10insTCATCATT XP_006724729.1:n.6101-11_6101-10insTCATCATT
XM_006724667.3:c.5939-11_5939-10insTCATCATT XP_006724730.1:n.5939-11_5939-10insTCATCATT
XM_017029601.2:c.6128-11_6128-10insTCATCATT XP_016885090.1:n.6128-11_6128-10insTCATCATT
XM_017029602.1:c.6098-11_6098-10insTCATCATT XP_016885091.1:n.6098-11_6098-10insTCATCATT
XM_017029603.1:c.6050-11_6050-10insTCATCATT XP_016885092.1:n.6050-11_6050-10insTCATCATT
XM_017029604.2:c.6017-11_6017-10insTCATCATT XP_016885093.1:n.6017-11_6017-10insTCATCATT
XM_017029605.1:c.6014-11_6014-10insTCATCATT XP_016885094.1:n.6014-11_6014-10insTCATCATT
XM_017029606.2:c.5987-11_5987-10insTCATCATT XP_016885095.1:n.5987-11_5987-10insTCATCATT
XM_017029607.2:c.5984-11_5984-10insTCATCATT XP_016885096.1:n.5984-11_5984-10insTCATCATT
XM_017029608.2:c.5936-11_5936-10insTCATCATT XP_016885097.1:n.5936-11_5936-10insTCATCATT
XM_017029609.1:c.5900-11_5900-10insTCATCATT XP_016885098.1:n.5900-11_5900-10insTCATCATT
XM_017029610.1:c.5897-11_5897-10insTCATCATT XP_016885099.1:n.5897-11_5897-10insTCATCATT
XM_017029611.1:c.5852-11_5852-10insTCATCATT XP_016885100.1:n.5852-11_5852-10insTCATCATT
XR_001755700.2:n.6517-11_6517-10insTCATCATT
NM_138270.4:c.6104-11_6104-10insTCATCATT NP_612114.2:n.6104-11_6104-10insTCATCATT
NM_000489.6:c.6218-11_6218-10insTCATCATT MANE Select NP_000480.3:n.6218-11_6218-10insTCATCATT
NM_138270.5:c.6104-11_6104-10insTCATCATT NP_612114.2:n.6104-11_6104-10insTCATCATT