Canonical Allele Identifier: CA2438929055
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508503T= , CM000685.2:g.77508503T= GRCh38
NC_000023.10:g.76763981T= , CM000685.1:g.76763981T= GRCh37
NC_000023.9:g.76650637T= NCBI36
NG_008838.2:g.282719A=
NG_008838.3:g.282767A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7327A= MANE Select ENSP00000362441.4:p.Asn2443=
ENST00000675732.1:c.2425A= ENSP00000502598.1:p.Asn809=
ENST00000373344.9:c.7327A= ENSP00000362441.4:p.Asn2443=
ENST00000395603.7:c.7213A= ENSP00000378967.3:p.Asn2405=
ENST00000480283.5:c.*6955A= ENSP00000480196.1:n.*6955A=
ENST00000623706.3:n.5647A=
ENST00000624766.1:n.558A=
NM_000489.4:c.7327A= NP_000480.3:p.Asn2443=
NM_138270.3:c.7213A= NP_612114.2:p.Asn2405=
XM_005262153.3:c.7324A= XP_005262210.2:p.Asn2442=
XM_005262154.3:c.7240A= XP_005262211.2:p.Asn2414=
XM_005262155.3:c.7210A= XP_005262212.2:p.Asn2404=
XM_005262156.3:c.7162A= XP_005262213.2:p.Asn2388=
XM_005262157.3:c.7123A= XP_005262214.2:p.Asn2375=
XM_006724666.2:c.7210A= XP_006724729.1:p.Asn2404=
XM_006724667.2:c.7048A= XP_006724730.1:p.Asn2350=
XR_938400.1:n.8919A=
NM_000489.5:c.7327A= NP_000480.3:p.Asn2443=
XM_005262153.5:c.7324A= XP_005262210.2:p.Asn2442=
XM_005262154.5:c.7240A= XP_005262211.2:p.Asn2414=
XM_005262155.4:c.7210A= XP_005262212.2:p.Asn2404=
XM_005262156.4:c.7162A= XP_005262213.2:p.Asn2388=
XM_005262157.5:c.7123A= XP_005262214.2:p.Asn2375=
XM_006724666.4:c.7210A= XP_006724729.1:p.Asn2404=
XM_006724667.3:c.7048A= XP_006724730.1:p.Asn2350=
XM_017029601.2:c.7237A= XP_016885090.1:p.Asn2413=
XM_017029602.1:c.7207A= XP_016885091.1:p.Asn2403=
XM_017029603.1:c.7159A= XP_016885092.1:p.Asn2387=
XM_017029604.2:c.7126A= XP_016885093.1:p.Asn2376=
XM_017029605.1:c.7123A= XP_016885094.1:p.Asn2375=
XM_017029606.2:c.7096A= XP_016885095.1:p.Asn2366=
XM_017029607.2:c.7093A= XP_016885096.1:p.Asn2365=
XM_017029608.2:c.7045A= XP_016885097.1:p.Asn2349=
XM_017029609.1:c.7009A= XP_016885098.1:p.Asn2337=
XM_017029610.1:c.7006A= XP_016885099.1:p.Asn2336=
XM_017029611.1:c.6961A= XP_016885100.1:p.Asn2321=
XR_001755700.2:n.7626A=
NM_138270.4:c.7213A= NP_612114.2:p.Asn2405=
NM_000489.6:c.7327A= MANE Select NP_000480.3:p.Asn2443=
NM_138270.5:c.7213A= NP_612114.2:p.Asn2405=