Canonical Allele Identifier: CA2438933057
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77520815G= , CM000685.2:g.77520815G= GRCh38
NC_000023.10:g.76776293G= , CM000685.1:g.76776293G= GRCh37
NC_000023.9:g.76662949G= NCBI36
NG_008838.2:g.270407C=
NG_008838.3:g.270455C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7173C= MANE Select ENSP00000362441.4:p.Tyr2391=
ENST00000675732.1:c.2271C= ENSP00000502598.1:p.Tyr757=
ENST00000373344.9:c.7173C= ENSP00000362441.4:p.Tyr2391=
ENST00000395603.7:c.7059C= ENSP00000378967.3:p.Tyr2353=
ENST00000480283.5:c.*6801C= ENSP00000480196.1:n.*6801C=
ENST00000623706.3:n.5493C=
ENST00000624766.1:n.404C=
NM_000489.4:c.7173C= NP_000480.3:p.Tyr2391=
NM_138270.3:c.7059C= NP_612114.2:p.Tyr2353=
XM_005262153.3:c.7170C= XP_005262210.2:p.Tyr2390=
XM_005262154.3:c.7086C= XP_005262211.2:p.Tyr2362=
XM_005262155.3:c.7056C= XP_005262212.2:p.Tyr2352=
XM_005262156.3:c.7008C= XP_005262213.2:p.Tyr2336=
XM_005262157.3:c.6969C= XP_005262214.2:p.Tyr2323=
XM_006724666.2:c.7056C= XP_006724729.1:p.Tyr2352=
XM_006724667.2:c.6894C= XP_006724730.1:p.Tyr2298=
XR_938400.1:n.8765C=
NM_000489.5:c.7173C= NP_000480.3:p.Tyr2391=
XM_005262153.5:c.7170C= XP_005262210.2:p.Tyr2390=
XM_005262154.5:c.7086C= XP_005262211.2:p.Tyr2362=
XM_005262155.4:c.7056C= XP_005262212.2:p.Tyr2352=
XM_005262156.4:c.7008C= XP_005262213.2:p.Tyr2336=
XM_005262157.5:c.6969C= XP_005262214.2:p.Tyr2323=
XM_006724666.4:c.7056C= XP_006724729.1:p.Tyr2352=
XM_006724667.3:c.6894C= XP_006724730.1:p.Tyr2298=
XM_017029601.2:c.7083C= XP_016885090.1:p.Tyr2361=
XM_017029602.1:c.7053C= XP_016885091.1:p.Tyr2351=
XM_017029603.1:c.7005C= XP_016885092.1:p.Tyr2335=
XM_017029604.2:c.6972C= XP_016885093.1:p.Tyr2324=
XM_017029605.1:c.6969C= XP_016885094.1:p.Tyr2323=
XM_017029606.2:c.6942C= XP_016885095.1:p.Tyr2314=
XM_017029607.2:c.6939C= XP_016885096.1:p.Tyr2313=
XM_017029608.2:c.6891C= XP_016885097.1:p.Tyr2297=
XM_017029609.1:c.6855C= XP_016885098.1:p.Tyr2285=
XM_017029610.1:c.6852C= XP_016885099.1:p.Tyr2284=
XM_017029611.1:c.6807C= XP_016885100.1:p.Tyr2269=
XR_001755700.2:n.7472C=
NM_138270.4:c.7059C= NP_612114.2:p.Tyr2353=
NM_000489.6:c.7173C= MANE Select NP_000480.3:p.Tyr2391=
NM_138270.5:c.7059C= NP_612114.2:p.Tyr2353=