Canonical Allele Identifier: CA2438929069
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508574T= , CM000685.2:g.77508574T= GRCh38
NC_000023.10:g.76764052T= , CM000685.1:g.76764052T= GRCh37
NC_000023.9:g.76650708T= NCBI36
NG_008838.2:g.282648A=
NG_008838.3:g.282696A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7256A= MANE Select ENSP00000362441.4:p.Asn2419=
ENST00000675732.1:c.2354A= ENSP00000502598.1:p.Asn785=
ENST00000373344.9:c.7256A= ENSP00000362441.4:p.Asn2419=
ENST00000395603.7:c.7142A= ENSP00000378967.3:p.Asn2381=
ENST00000480283.5:c.*6884A= ENSP00000480196.1:n.*6884A=
ENST00000623706.3:n.5576A=
ENST00000624766.1:n.487A=
NM_000489.4:c.7256A= NP_000480.3:p.Asn2419=
NM_138270.3:c.7142A= NP_612114.2:p.Asn2381=
XM_005262153.3:c.7253A= XP_005262210.2:p.Asn2418=
XM_005262154.3:c.7169A= XP_005262211.2:p.Asn2390=
XM_005262155.3:c.7139A= XP_005262212.2:p.Asn2380=
XM_005262156.3:c.7091A= XP_005262213.2:p.Asn2364=
XM_005262157.3:c.7052A= XP_005262214.2:p.Asn2351=
XM_006724666.2:c.7139A= XP_006724729.1:p.Asn2380=
XM_006724667.2:c.6977A= XP_006724730.1:p.Asn2326=
XR_938400.1:n.8848A=
NM_000489.5:c.7256A= NP_000480.3:p.Asn2419=
XM_005262153.5:c.7253A= XP_005262210.2:p.Asn2418=
XM_005262154.5:c.7169A= XP_005262211.2:p.Asn2390=
XM_005262155.4:c.7139A= XP_005262212.2:p.Asn2380=
XM_005262156.4:c.7091A= XP_005262213.2:p.Asn2364=
XM_005262157.5:c.7052A= XP_005262214.2:p.Asn2351=
XM_006724666.4:c.7139A= XP_006724729.1:p.Asn2380=
XM_006724667.3:c.6977A= XP_006724730.1:p.Asn2326=
XM_017029601.2:c.7166A= XP_016885090.1:p.Asn2389=
XM_017029602.1:c.7136A= XP_016885091.1:p.Asn2379=
XM_017029603.1:c.7088A= XP_016885092.1:p.Asn2363=
XM_017029604.2:c.7055A= XP_016885093.1:p.Asn2352=
XM_017029605.1:c.7052A= XP_016885094.1:p.Asn2351=
XM_017029606.2:c.7025A= XP_016885095.1:p.Asn2342=
XM_017029607.2:c.7022A= XP_016885096.1:p.Asn2341=
XM_017029608.2:c.6974A= XP_016885097.1:p.Asn2325=
XM_017029609.1:c.6938A= XP_016885098.1:p.Asn2313=
XM_017029610.1:c.6935A= XP_016885099.1:p.Asn2312=
XM_017029611.1:c.6890A= XP_016885100.1:p.Asn2297=
XR_001755700.2:n.7555A=
NM_138270.4:c.7142A= NP_612114.2:p.Asn2381=
NM_000489.6:c.7256A= MANE Select NP_000480.3:p.Asn2419=
NM_138270.5:c.7142A= NP_612114.2:p.Asn2381=