Canonical Allele Identifier: CA2438929026
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508397G= , CM000685.2:g.77508397G= GRCh38
NC_000023.10:g.76763875G= , CM000685.1:g.76763875G= GRCh37
NC_000023.9:g.76650531G= NCBI36
NG_008838.2:g.282825C=
NG_008838.3:g.282873C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7433C= MANE Select ENSP00000362441.4:p.Pro2478=
ENST00000675732.1:c.2531C= ENSP00000502598.1:p.Pro844=
ENST00000373344.9:c.7433C= ENSP00000362441.4:p.Pro2478=
ENST00000395603.7:c.7319C= ENSP00000378967.3:p.Pro2440=
ENST00000480283.5:c.*7061C= ENSP00000480196.1:n.*7061C=
ENST00000623706.3:n.5753C=
NM_000489.4:c.7433C= NP_000480.3:p.Pro2478=
NM_138270.3:c.7319C= NP_612114.2:p.Pro2440=
XM_005262153.3:c.7430C= XP_005262210.2:p.Pro2477=
XM_005262154.3:c.7346C= XP_005262211.2:p.Pro2449=
XM_005262155.3:c.7316C= XP_005262212.2:p.Pro2439=
XM_005262156.3:c.7268C= XP_005262213.2:p.Pro2423=
XM_005262157.3:c.7229C= XP_005262214.2:p.Pro2410=
XM_006724666.2:c.7316C= XP_006724729.1:p.Pro2439=
XM_006724667.2:c.7154C= XP_006724730.1:p.Pro2385=
XR_938400.1:n.9025C=
NM_000489.5:c.7433C= NP_000480.3:p.Pro2478=
XM_005262153.5:c.7430C= XP_005262210.2:p.Pro2477=
XM_005262154.5:c.7346C= XP_005262211.2:p.Pro2449=
XM_005262155.4:c.7316C= XP_005262212.2:p.Pro2439=
XM_005262156.4:c.7268C= XP_005262213.2:p.Pro2423=
XM_005262157.5:c.7229C= XP_005262214.2:p.Pro2410=
XM_006724666.4:c.7316C= XP_006724729.1:p.Pro2439=
XM_006724667.3:c.7154C= XP_006724730.1:p.Pro2385=
XM_017029601.2:c.7343C= XP_016885090.1:p.Pro2448=
XM_017029602.1:c.7313C= XP_016885091.1:p.Pro2438=
XM_017029603.1:c.7265C= XP_016885092.1:p.Pro2422=
XM_017029604.2:c.7232C= XP_016885093.1:p.Pro2411=
XM_017029605.1:c.7229C= XP_016885094.1:p.Pro2410=
XM_017029606.2:c.7202C= XP_016885095.1:p.Pro2401=
XM_017029607.2:c.7199C= XP_016885096.1:p.Pro2400=
XM_017029608.2:c.7151C= XP_016885097.1:p.Pro2384=
XM_017029609.1:c.7115C= XP_016885098.1:p.Pro2372=
XM_017029610.1:c.7112C= XP_016885099.1:p.Pro2371=
XM_017029611.1:c.7067C= XP_016885100.1:p.Pro2356=
XR_001755700.2:n.7732C=
NM_138270.4:c.7319C= NP_612114.2:p.Pro2440=
NM_000489.6:c.7433C= MANE Select NP_000480.3:p.Pro2478=
NM_138270.5:c.7319C= NP_612114.2:p.Pro2440=