Canonical Allele Identifier: CA2438929051
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508494T= , CM000685.2:g.77508494T= GRCh38
NC_000023.10:g.76763972T= , CM000685.1:g.76763972T= GRCh37
NC_000023.9:g.76650628T= NCBI36
NG_008838.2:g.282728A=
NG_008838.3:g.282776A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7336A= MANE Select ENSP00000362441.4:p.Met2446=
ENST00000675732.1:c.2434A= ENSP00000502598.1:p.Met812=
ENST00000373344.9:c.7336A= ENSP00000362441.4:p.Met2446=
ENST00000395603.7:c.7222A= ENSP00000378967.3:p.Met2408=
ENST00000480283.5:c.*6964A= ENSP00000480196.1:n.*6964A=
ENST00000623706.3:n.5656A=
ENST00000624766.1:n.567A=
NM_000489.4:c.7336A= NP_000480.3:p.Met2446=
NM_138270.3:c.7222A= NP_612114.2:p.Met2408=
XM_005262153.3:c.7333A= XP_005262210.2:p.Met2445=
XM_005262154.3:c.7249A= XP_005262211.2:p.Met2417=
XM_005262155.3:c.7219A= XP_005262212.2:p.Met2407=
XM_005262156.3:c.7171A= XP_005262213.2:p.Met2391=
XM_005262157.3:c.7132A= XP_005262214.2:p.Met2378=
XM_006724666.2:c.7219A= XP_006724729.1:p.Met2407=
XM_006724667.2:c.7057A= XP_006724730.1:p.Met2353=
XR_938400.1:n.8928A=
NM_000489.5:c.7336A= NP_000480.3:p.Met2446=
XM_005262153.5:c.7333A= XP_005262210.2:p.Met2445=
XM_005262154.5:c.7249A= XP_005262211.2:p.Met2417=
XM_005262155.4:c.7219A= XP_005262212.2:p.Met2407=
XM_005262156.4:c.7171A= XP_005262213.2:p.Met2391=
XM_005262157.5:c.7132A= XP_005262214.2:p.Met2378=
XM_006724666.4:c.7219A= XP_006724729.1:p.Met2407=
XM_006724667.3:c.7057A= XP_006724730.1:p.Met2353=
XM_017029601.2:c.7246A= XP_016885090.1:p.Met2416=
XM_017029602.1:c.7216A= XP_016885091.1:p.Met2406=
XM_017029603.1:c.7168A= XP_016885092.1:p.Met2390=
XM_017029604.2:c.7135A= XP_016885093.1:p.Met2379=
XM_017029605.1:c.7132A= XP_016885094.1:p.Met2378=
XM_017029606.2:c.7105A= XP_016885095.1:p.Met2369=
XM_017029607.2:c.7102A= XP_016885096.1:p.Met2368=
XM_017029608.2:c.7054A= XP_016885097.1:p.Met2352=
XM_017029609.1:c.7018A= XP_016885098.1:p.Met2340=
XM_017029610.1:c.7015A= XP_016885099.1:p.Met2339=
XM_017029611.1:c.6970A= XP_016885100.1:p.Met2324=
XR_001755700.2:n.7635A=
NM_138270.4:c.7222A= NP_612114.2:p.Met2408=
NM_000489.6:c.7336A= MANE Select NP_000480.3:p.Met2446=
NM_138270.5:c.7222A= NP_612114.2:p.Met2408=