Canonical Allele Identifier: CA2438929059
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508514G= , CM000685.2:g.77508514G= GRCh38
NC_000023.10:g.76763992G= , CM000685.1:g.76763992G= GRCh37
NC_000023.9:g.76650648G= NCBI36
NG_008838.2:g.282708C=
NG_008838.3:g.282756C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7316C= MANE Select ENSP00000362441.4:p.Pro2439=
ENST00000675732.1:c.2414C= ENSP00000502598.1:p.Pro805=
ENST00000373344.9:c.7316C= ENSP00000362441.4:p.Pro2439=
ENST00000395603.7:c.7202C= ENSP00000378967.3:p.Pro2401=
ENST00000480283.5:c.*6944C= ENSP00000480196.1:n.*6944C=
ENST00000623706.3:n.5636C=
ENST00000624766.1:n.547C=
NM_000489.4:c.7316C= NP_000480.3:p.Pro2439=
NM_138270.3:c.7202C= NP_612114.2:p.Pro2401=
XM_005262153.3:c.7313C= XP_005262210.2:p.Pro2438=
XM_005262154.3:c.7229C= XP_005262211.2:p.Pro2410=
XM_005262155.3:c.7199C= XP_005262212.2:p.Pro2400=
XM_005262156.3:c.7151C= XP_005262213.2:p.Pro2384=
XM_005262157.3:c.7112C= XP_005262214.2:p.Pro2371=
XM_006724666.2:c.7199C= XP_006724729.1:p.Pro2400=
XM_006724667.2:c.7037C= XP_006724730.1:p.Pro2346=
XR_938400.1:n.8908C=
NM_000489.5:c.7316C= NP_000480.3:p.Pro2439=
XM_005262153.5:c.7313C= XP_005262210.2:p.Pro2438=
XM_005262154.5:c.7229C= XP_005262211.2:p.Pro2410=
XM_005262155.4:c.7199C= XP_005262212.2:p.Pro2400=
XM_005262156.4:c.7151C= XP_005262213.2:p.Pro2384=
XM_005262157.5:c.7112C= XP_005262214.2:p.Pro2371=
XM_006724666.4:c.7199C= XP_006724729.1:p.Pro2400=
XM_006724667.3:c.7037C= XP_006724730.1:p.Pro2346=
XM_017029601.2:c.7226C= XP_016885090.1:p.Pro2409=
XM_017029602.1:c.7196C= XP_016885091.1:p.Pro2399=
XM_017029603.1:c.7148C= XP_016885092.1:p.Pro2383=
XM_017029604.2:c.7115C= XP_016885093.1:p.Pro2372=
XM_017029605.1:c.7112C= XP_016885094.1:p.Pro2371=
XM_017029606.2:c.7085C= XP_016885095.1:p.Pro2362=
XM_017029607.2:c.7082C= XP_016885096.1:p.Pro2361=
XM_017029608.2:c.7034C= XP_016885097.1:p.Pro2345=
XM_017029609.1:c.6998C= XP_016885098.1:p.Pro2333=
XM_017029610.1:c.6995C= XP_016885099.1:p.Pro2332=
XM_017029611.1:c.6950C= XP_016885100.1:p.Pro2317=
XR_001755700.2:n.7615C=
NM_138270.4:c.7202C= NP_612114.2:p.Pro2401=
NM_000489.6:c.7316C= MANE Select NP_000480.3:p.Pro2439=
NM_138270.5:c.7202C= NP_612114.2:p.Pro2401=