Canonical Allele Identifier: CA2438929023
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508391C= , CM000685.2:g.77508391C= GRCh38
NC_000023.10:g.76763869C= , CM000685.1:g.76763869C= GRCh37
NC_000023.9:g.76650525C= NCBI36
NG_008838.2:g.282831G=
NG_008838.3:g.282879G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7439G= MANE Select ENSP00000362441.4:p.Arg2480=
ENST00000675732.1:c.2537G= ENSP00000502598.1:p.Arg846=
ENST00000373344.9:c.7439G= ENSP00000362441.4:p.Arg2480=
ENST00000395603.7:c.7325G= ENSP00000378967.3:p.Arg2442=
ENST00000480283.5:c.*7067G= ENSP00000480196.1:n.*7067G=
ENST00000623706.3:n.5759G=
NM_000489.4:c.7439G= NP_000480.3:p.Arg2480=
NM_138270.3:c.7325G= NP_612114.2:p.Arg2442=
XM_005262153.3:c.7436G= XP_005262210.2:p.Arg2479=
XM_005262154.3:c.7352G= XP_005262211.2:p.Arg2451=
XM_005262155.3:c.7322G= XP_005262212.2:p.Arg2441=
XM_005262156.3:c.7274G= XP_005262213.2:p.Arg2425=
XM_005262157.3:c.7235G= XP_005262214.2:p.Arg2412=
XM_006724666.2:c.7322G= XP_006724729.1:p.Arg2441=
XM_006724667.2:c.7160G= XP_006724730.1:p.Arg2387=
XR_938400.1:n.9031G=
NM_000489.5:c.7439G= NP_000480.3:p.Arg2480=
XM_005262153.5:c.7436G= XP_005262210.2:p.Arg2479=
XM_005262154.5:c.7352G= XP_005262211.2:p.Arg2451=
XM_005262155.4:c.7322G= XP_005262212.2:p.Arg2441=
XM_005262156.4:c.7274G= XP_005262213.2:p.Arg2425=
XM_005262157.5:c.7235G= XP_005262214.2:p.Arg2412=
XM_006724666.4:c.7322G= XP_006724729.1:p.Arg2441=
XM_006724667.3:c.7160G= XP_006724730.1:p.Arg2387=
XM_017029601.2:c.7349G= XP_016885090.1:p.Arg2450=
XM_017029602.1:c.7319G= XP_016885091.1:p.Arg2440=
XM_017029603.1:c.7271G= XP_016885092.1:p.Arg2424=
XM_017029604.2:c.7238G= XP_016885093.1:p.Arg2413=
XM_017029605.1:c.7235G= XP_016885094.1:p.Arg2412=
XM_017029606.2:c.7208G= XP_016885095.1:p.Arg2403=
XM_017029607.2:c.7205G= XP_016885096.1:p.Arg2402=
XM_017029608.2:c.7157G= XP_016885097.1:p.Arg2386=
XM_017029609.1:c.7121G= XP_016885098.1:p.Arg2374=
XM_017029610.1:c.7118G= XP_016885099.1:p.Arg2373=
XM_017029611.1:c.7073G= XP_016885100.1:p.Arg2358=
XR_001755700.2:n.7738G=
NM_138270.4:c.7325G= NP_612114.2:p.Arg2442=
NM_000489.6:c.7439G= MANE Select NP_000480.3:p.Arg2480=
NM_138270.5:c.7325G= NP_612114.2:p.Arg2442=