Canonical Allele Identifier: CA2438929037
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508431T= , CM000685.2:g.77508431T= GRCh38
NC_000023.10:g.76763909T= , CM000685.1:g.76763909T= GRCh37
NC_000023.9:g.76650565T= NCBI36
NG_008838.2:g.282791A=
NG_008838.3:g.282839A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7399A= MANE Select ENSP00000362441.4:p.Met2467=
ENST00000675732.1:c.2497A= ENSP00000502598.1:p.Met833=
ENST00000373344.9:c.7399A= ENSP00000362441.4:p.Met2467=
ENST00000395603.7:c.7285A= ENSP00000378967.3:p.Met2429=
ENST00000480283.5:c.*7027A= ENSP00000480196.1:n.*7027A=
ENST00000623706.3:n.5719A=
NM_000489.4:c.7399A= NP_000480.3:p.Met2467=
NM_138270.3:c.7285A= NP_612114.2:p.Met2429=
XM_005262153.3:c.7396A= XP_005262210.2:p.Met2466=
XM_005262154.3:c.7312A= XP_005262211.2:p.Met2438=
XM_005262155.3:c.7282A= XP_005262212.2:p.Met2428=
XM_005262156.3:c.7234A= XP_005262213.2:p.Met2412=
XM_005262157.3:c.7195A= XP_005262214.2:p.Met2399=
XM_006724666.2:c.7282A= XP_006724729.1:p.Met2428=
XM_006724667.2:c.7120A= XP_006724730.1:p.Met2374=
XR_938400.1:n.8991A=
NM_000489.5:c.7399A= NP_000480.3:p.Met2467=
XM_005262153.5:c.7396A= XP_005262210.2:p.Met2466=
XM_005262154.5:c.7312A= XP_005262211.2:p.Met2438=
XM_005262155.4:c.7282A= XP_005262212.2:p.Met2428=
XM_005262156.4:c.7234A= XP_005262213.2:p.Met2412=
XM_005262157.5:c.7195A= XP_005262214.2:p.Met2399=
XM_006724666.4:c.7282A= XP_006724729.1:p.Met2428=
XM_006724667.3:c.7120A= XP_006724730.1:p.Met2374=
XM_017029601.2:c.7309A= XP_016885090.1:p.Met2437=
XM_017029602.1:c.7279A= XP_016885091.1:p.Met2427=
XM_017029603.1:c.7231A= XP_016885092.1:p.Met2411=
XM_017029604.2:c.7198A= XP_016885093.1:p.Met2400=
XM_017029605.1:c.7195A= XP_016885094.1:p.Met2399=
XM_017029606.2:c.7168A= XP_016885095.1:p.Met2390=
XM_017029607.2:c.7165A= XP_016885096.1:p.Met2389=
XM_017029608.2:c.7117A= XP_016885097.1:p.Met2373=
XM_017029609.1:c.7081A= XP_016885098.1:p.Met2361=
XM_017029610.1:c.7078A= XP_016885099.1:p.Met2360=
XM_017029611.1:c.7033A= XP_016885100.1:p.Met2345=
XR_001755700.2:n.7698A=
NM_138270.4:c.7285A= NP_612114.2:p.Met2429=
NM_000489.6:c.7399A= MANE Select NP_000480.3:p.Met2467=
NM_138270.5:c.7285A= NP_612114.2:p.Met2429=