Canonical Allele Identifier: CA2438929052
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508495G= , CM000685.2:g.77508495G= GRCh38
NC_000023.10:g.76763973G= , CM000685.1:g.76763973G= GRCh37
NC_000023.9:g.76650629G= NCBI36
NG_008838.2:g.282727C=
NG_008838.3:g.282775C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7335C= MANE Select ENSP00000362441.4:p.Ile2445=
ENST00000675732.1:c.2433C= ENSP00000502598.1:p.Ile811=
ENST00000373344.9:c.7335C= ENSP00000362441.4:p.Ile2445=
ENST00000395603.7:c.7221C= ENSP00000378967.3:p.Ile2407=
ENST00000480283.5:c.*6963C= ENSP00000480196.1:n.*6963C=
ENST00000623706.3:n.5655C=
ENST00000624766.1:n.566C=
NM_000489.4:c.7335C= NP_000480.3:p.Ile2445=
NM_138270.3:c.7221C= NP_612114.2:p.Ile2407=
XM_005262153.3:c.7332C= XP_005262210.2:p.Ile2444=
XM_005262154.3:c.7248C= XP_005262211.2:p.Ile2416=
XM_005262155.3:c.7218C= XP_005262212.2:p.Ile2406=
XM_005262156.3:c.7170C= XP_005262213.2:p.Ile2390=
XM_005262157.3:c.7131C= XP_005262214.2:p.Ile2377=
XM_006724666.2:c.7218C= XP_006724729.1:p.Ile2406=
XM_006724667.2:c.7056C= XP_006724730.1:p.Ile2352=
XR_938400.1:n.8927C=
NM_000489.5:c.7335C= NP_000480.3:p.Ile2445=
XM_005262153.5:c.7332C= XP_005262210.2:p.Ile2444=
XM_005262154.5:c.7248C= XP_005262211.2:p.Ile2416=
XM_005262155.4:c.7218C= XP_005262212.2:p.Ile2406=
XM_005262156.4:c.7170C= XP_005262213.2:p.Ile2390=
XM_005262157.5:c.7131C= XP_005262214.2:p.Ile2377=
XM_006724666.4:c.7218C= XP_006724729.1:p.Ile2406=
XM_006724667.3:c.7056C= XP_006724730.1:p.Ile2352=
XM_017029601.2:c.7245C= XP_016885090.1:p.Ile2415=
XM_017029602.1:c.7215C= XP_016885091.1:p.Ile2405=
XM_017029603.1:c.7167C= XP_016885092.1:p.Ile2389=
XM_017029604.2:c.7134C= XP_016885093.1:p.Ile2378=
XM_017029605.1:c.7131C= XP_016885094.1:p.Ile2377=
XM_017029606.2:c.7104C= XP_016885095.1:p.Ile2368=
XM_017029607.2:c.7101C= XP_016885096.1:p.Ile2367=
XM_017029608.2:c.7053C= XP_016885097.1:p.Ile2351=
XM_017029609.1:c.7017C= XP_016885098.1:p.Ile2339=
XM_017029610.1:c.7014C= XP_016885099.1:p.Ile2338=
XM_017029611.1:c.6969C= XP_016885100.1:p.Ile2323=
XR_001755700.2:n.7634C=
NM_138270.4:c.7221C= NP_612114.2:p.Ile2407=
NM_000489.6:c.7335C= MANE Select NP_000480.3:p.Ile2445=
NM_138270.5:c.7221C= NP_612114.2:p.Ile2407=