Canonical Allele Identifier: CA2438951396
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77574303A= , CM000685.2:g.77574303A= GRCh38
NC_000023.10:g.76829768A= , CM000685.1:g.76829768A= GRCh37
NC_000023.9:g.76716424A= NCBI36
NG_008838.2:g.216919T=
NG_008838.3:g.216967T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.6273T= MANE Select ENSP00000362441.4:p.Thr2091=
ENST00000675732.1:c.1371T= ENSP00000502598.1:p.Thr457=
ENST00000373344.9:c.6273T= ENSP00000362441.4:p.Thr2091=
ENST00000395603.7:c.6159T= ENSP00000378967.3:p.Thr2053=
ENST00000480283.5:c.*5901T= ENSP00000480196.1:n.*5901T=
ENST00000623316.1:c.757T=
ENST00000623706.3:n.3343T=
NM_000489.4:c.6273T= NP_000480.3:p.Thr2091=
NM_138270.3:c.6159T= NP_612114.2:p.Thr2053=
XM_005262153.3:c.6270T= XP_005262210.2:p.Thr2090=
XM_005262154.3:c.6186T= XP_005262211.2:p.Thr2062=
XM_005262155.3:c.6156T= XP_005262212.2:p.Thr2052=
XM_005262156.3:c.6108T= XP_005262213.2:p.Thr2036=
XM_005262157.3:c.6069T= XP_005262214.2:p.Thr2023=
XM_006724666.2:c.6156T= XP_006724729.1:p.Thr2052=
XM_006724667.2:c.5994T= XP_006724730.1:p.Thr1998=
XR_938400.1:n.6615T=
NM_000489.5:c.6273T= NP_000480.3:p.Thr2091=
XM_005262153.5:c.6270T= XP_005262210.2:p.Thr2090=
XM_005262154.5:c.6186T= XP_005262211.2:p.Thr2062=
XM_005262155.4:c.6156T= XP_005262212.2:p.Thr2052=
XM_005262156.4:c.6108T= XP_005262213.2:p.Thr2036=
XM_005262157.5:c.6069T= XP_005262214.2:p.Thr2023=
XM_006724666.4:c.6156T= XP_006724729.1:p.Thr2052=
XM_006724667.3:c.5994T= XP_006724730.1:p.Thr1998=
XM_017029601.2:c.6183T= XP_016885090.1:p.Thr2061=
XM_017029602.1:c.6153T= XP_016885091.1:p.Thr2051=
XM_017029603.1:c.6105T= XP_016885092.1:p.Thr2035=
XM_017029604.2:c.6072T= XP_016885093.1:p.Thr2024=
XM_017029605.1:c.6069T= XP_016885094.1:p.Thr2023=
XM_017029606.2:c.6042T= XP_016885095.1:p.Thr2014=
XM_017029607.2:c.6039T= XP_016885096.1:p.Thr2013=
XM_017029608.2:c.5991T= XP_016885097.1:p.Thr1997=
XM_017029609.1:c.5955T= XP_016885098.1:p.Thr1985=
XM_017029610.1:c.5952T= XP_016885099.1:p.Thr1984=
XM_017029611.1:c.5907T= XP_016885100.1:p.Thr1969=
XR_001755700.2:n.6572T=
NM_138270.4:c.6159T= NP_612114.2:p.Thr2053=
NM_000489.6:c.6273T= MANE Select NP_000480.3:p.Thr2091=
NM_138270.5:c.6159T= NP_612114.2:p.Thr2053=