Canonical Allele Identifier: CA2438951472
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77574512G= , CM000685.2:g.77574512G= GRCh38
NC_000023.10:g.76829977G= , CM000685.1:g.76829977G= GRCh37
NC_000023.9:g.76716633G= NCBI36
NG_008838.2:g.216710C=
NG_008838.3:g.216758C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.6218-154C= MANE Select ENSP00000362441.4:n.6218-154C=
ENST00000636152.1:n.53-154C=
ENST00000675732.1:c.1316-154C= ENSP00000502598.1:n.1316-154C=
ENST00000373344.9:c.6218-154C= ENSP00000362441.4:n.6218-154C=
ENST00000395603.7:c.6104-154C= ENSP00000378967.3:n.6104-154C=
ENST00000480283.5:c.*5846-154C= ENSP00000480196.1:n.*5846-154C=
ENST00000623316.1:c.702-154C=
ENST00000623706.3:n.3288-154C=
NM_000489.4:c.6218-154C= NP_000480.3:n.6218-154C=
NM_138270.3:c.6104-154C= NP_612114.2:n.6104-154C=
XM_005262153.3:c.6215-154C= XP_005262210.2:n.6215-154C=
XM_005262154.3:c.6131-154C= XP_005262211.2:n.6131-154C=
XM_005262155.3:c.6101-154C= XP_005262212.2:n.6101-154C=
XM_005262156.3:c.6053-154C= XP_005262213.2:n.6053-154C=
XM_005262157.3:c.6014-154C= XP_005262214.2:n.6014-154C=
XM_006724666.2:c.6101-154C= XP_006724729.1:n.6101-154C=
XM_006724667.2:c.5939-154C= XP_006724730.1:n.5939-154C=
XR_938400.1:n.6560-154C=
NM_000489.5:c.6218-154C= NP_000480.3:n.6218-154C=
XM_005262153.5:c.6215-154C= XP_005262210.2:n.6215-154C=
XM_005262154.5:c.6131-154C= XP_005262211.2:n.6131-154C=
XM_005262155.4:c.6101-154C= XP_005262212.2:n.6101-154C=
XM_005262156.4:c.6053-154C= XP_005262213.2:n.6053-154C=
XM_005262157.5:c.6014-154C= XP_005262214.2:n.6014-154C=
XM_006724666.4:c.6101-154C= XP_006724729.1:n.6101-154C=
XM_006724667.3:c.5939-154C= XP_006724730.1:n.5939-154C=
XM_017029601.2:c.6128-154C= XP_016885090.1:n.6128-154C=
XM_017029602.1:c.6098-154C= XP_016885091.1:n.6098-154C=
XM_017029603.1:c.6050-154C= XP_016885092.1:n.6050-154C=
XM_017029604.2:c.6017-154C= XP_016885093.1:n.6017-154C=
XM_017029605.1:c.6014-154C= XP_016885094.1:n.6014-154C=
XM_017029606.2:c.5987-154C= XP_016885095.1:n.5987-154C=
XM_017029607.2:c.5984-154C= XP_016885096.1:n.5984-154C=
XM_017029608.2:c.5936-154C= XP_016885097.1:n.5936-154C=
XM_017029609.1:c.5900-154C= XP_016885098.1:n.5900-154C=
XM_017029610.1:c.5897-154C= XP_016885099.1:n.5897-154C=
XM_017029611.1:c.5852-154C= XP_016885100.1:n.5852-154C=
XR_001755700.2:n.6517-154C=
NM_138270.4:c.6104-154C= NP_612114.2:n.6104-154C=
NM_000489.6:c.6218-154C= MANE Select NP_000480.3:n.6218-154C=
NM_138270.5:c.6104-154C= NP_612114.2:n.6104-154C=