Canonical Allele Identifier: CA2438951458
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77574480A= , CM000685.2:g.77574480A= GRCh38
NC_000023.10:g.76829945A= , CM000685.1:g.76829945A= GRCh37
NC_000023.9:g.76716601A= NCBI36
NG_008838.2:g.216742T=
NG_008838.3:g.216790T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.6218-122T= MANE Select ENSP00000362441.4:n.6218-122T=
ENST00000636152.1:n.53-122T=
ENST00000675732.1:c.1316-122T= ENSP00000502598.1:n.1316-122T=
ENST00000373344.9:c.6218-122T= ENSP00000362441.4:n.6218-122T=
ENST00000395603.7:c.6104-122T= ENSP00000378967.3:n.6104-122T=
ENST00000480283.5:c.*5846-122T= ENSP00000480196.1:n.*5846-122T=
ENST00000623316.1:c.702-122T=
ENST00000623706.3:n.3288-122T=
NM_000489.4:c.6218-122T= NP_000480.3:n.6218-122T=
NM_138270.3:c.6104-122T= NP_612114.2:n.6104-122T=
XM_005262153.3:c.6215-122T= XP_005262210.2:n.6215-122T=
XM_005262154.3:c.6131-122T= XP_005262211.2:n.6131-122T=
XM_005262155.3:c.6101-122T= XP_005262212.2:n.6101-122T=
XM_005262156.3:c.6053-122T= XP_005262213.2:n.6053-122T=
XM_005262157.3:c.6014-122T= XP_005262214.2:n.6014-122T=
XM_006724666.2:c.6101-122T= XP_006724729.1:n.6101-122T=
XM_006724667.2:c.5939-122T= XP_006724730.1:n.5939-122T=
XR_938400.1:n.6560-122T=
NM_000489.5:c.6218-122T= NP_000480.3:n.6218-122T=
XM_005262153.5:c.6215-122T= XP_005262210.2:n.6215-122T=
XM_005262154.5:c.6131-122T= XP_005262211.2:n.6131-122T=
XM_005262155.4:c.6101-122T= XP_005262212.2:n.6101-122T=
XM_005262156.4:c.6053-122T= XP_005262213.2:n.6053-122T=
XM_005262157.5:c.6014-122T= XP_005262214.2:n.6014-122T=
XM_006724666.4:c.6101-122T= XP_006724729.1:n.6101-122T=
XM_006724667.3:c.5939-122T= XP_006724730.1:n.5939-122T=
XM_017029601.2:c.6128-122T= XP_016885090.1:n.6128-122T=
XM_017029602.1:c.6098-122T= XP_016885091.1:n.6098-122T=
XM_017029603.1:c.6050-122T= XP_016885092.1:n.6050-122T=
XM_017029604.2:c.6017-122T= XP_016885093.1:n.6017-122T=
XM_017029605.1:c.6014-122T= XP_016885094.1:n.6014-122T=
XM_017029606.2:c.5987-122T= XP_016885095.1:n.5987-122T=
XM_017029607.2:c.5984-122T= XP_016885096.1:n.5984-122T=
XM_017029608.2:c.5936-122T= XP_016885097.1:n.5936-122T=
XM_017029609.1:c.5900-122T= XP_016885098.1:n.5900-122T=
XM_017029610.1:c.5897-122T= XP_016885099.1:n.5897-122T=
XM_017029611.1:c.5852-122T= XP_016885100.1:n.5852-122T=
XR_001755700.2:n.6517-122T=
NM_138270.4:c.6104-122T= NP_612114.2:n.6104-122T=
NM_000489.6:c.6218-122T= MANE Select NP_000480.3:n.6218-122T=
NM_138270.5:c.6104-122T= NP_612114.2:n.6104-122T=