Canonical Allele Identifier: CA2438933074
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77520893T= , CM000685.2:g.77520893T= GRCh38
NC_000023.10:g.76776371T= , CM000685.1:g.76776371T= GRCh37
NC_000023.9:g.76663027T= NCBI36
NG_008838.2:g.270329A=
NG_008838.3:g.270377A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7095A= MANE Select ENSP00000362441.4:p.Ser2365=
ENST00000675732.1:c.2193A= ENSP00000502598.1:p.Ser731=
ENST00000373344.9:c.7095A= ENSP00000362441.4:p.Ser2365=
ENST00000395603.7:c.6981A= ENSP00000378967.3:p.Ser2327=
ENST00000480283.5:c.*6723A= ENSP00000480196.1:n.*6723A=
ENST00000623706.3:n.5415A=
ENST00000624766.1:n.326A=
NM_000489.4:c.7095A= NP_000480.3:p.Ser2365=
NM_138270.3:c.6981A= NP_612114.2:p.Ser2327=
XM_005262153.3:c.7092A= XP_005262210.2:p.Ser2364=
XM_005262154.3:c.7008A= XP_005262211.2:p.Ser2336=
XM_005262155.3:c.6978A= XP_005262212.2:p.Ser2326=
XM_005262156.3:c.6930A= XP_005262213.2:p.Ser2310=
XM_005262157.3:c.6891A= XP_005262214.2:p.Ser2297=
XM_006724666.2:c.6978A= XP_006724729.1:p.Ser2326=
XM_006724667.2:c.6816A= XP_006724730.1:p.Ser2272=
XR_938400.1:n.8687A=
NM_000489.5:c.7095A= NP_000480.3:p.Ser2365=
XM_005262153.5:c.7092A= XP_005262210.2:p.Ser2364=
XM_005262154.5:c.7008A= XP_005262211.2:p.Ser2336=
XM_005262155.4:c.6978A= XP_005262212.2:p.Ser2326=
XM_005262156.4:c.6930A= XP_005262213.2:p.Ser2310=
XM_005262157.5:c.6891A= XP_005262214.2:p.Ser2297=
XM_006724666.4:c.6978A= XP_006724729.1:p.Ser2326=
XM_006724667.3:c.6816A= XP_006724730.1:p.Ser2272=
XM_017029601.2:c.7005A= XP_016885090.1:p.Ser2335=
XM_017029602.1:c.6975A= XP_016885091.1:p.Ser2325=
XM_017029603.1:c.6927A= XP_016885092.1:p.Ser2309=
XM_017029604.2:c.6894A= XP_016885093.1:p.Ser2298=
XM_017029605.1:c.6891A= XP_016885094.1:p.Ser2297=
XM_017029606.2:c.6864A= XP_016885095.1:p.Ser2288=
XM_017029607.2:c.6861A= XP_016885096.1:p.Ser2287=
XM_017029608.2:c.6813A= XP_016885097.1:p.Ser2271=
XM_017029609.1:c.6777A= XP_016885098.1:p.Ser2259=
XM_017029610.1:c.6774A= XP_016885099.1:p.Ser2258=
XM_017029611.1:c.6729A= XP_016885100.1:p.Ser2243=
XR_001755700.2:n.7394A=
NM_138270.4:c.6981A= NP_612114.2:p.Ser2327=
NM_000489.6:c.7095A= MANE Select NP_000480.3:p.Ser2365=
NM_138270.5:c.6981A= NP_612114.2:p.Ser2327=