Canonical Allele Identifier: CA2438951408

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574356C= , CM000685.2:g.77574356C=	GRCh38
NC_000023.10:g.76829821C= , CM000685.1:g.76829821C=	GRCh37
NC_000023.9:g.76716477C=	NCBI36
NG_008838.2:g.216866G=
NG_008838.3:g.216914G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6220G= MANE Select	ENSP00000362441.4:p.Glu2074=
ENST00000636152.1:n.55G=
ENST00000675732.1:c.1318G=	ENSP00000502598.1:p.Glu440=
ENST00000373344.9:c.6220G=	ENSP00000362441.4:p.Glu2074=
ENST00000395603.7:c.6106G=	ENSP00000378967.3:p.Glu2036=
ENST00000480283.5:c.*5848G=	ENSP00000480196.1:n.*5848G=
ENST00000623316.1:c.704G=
ENST00000623706.3:n.3290G=
NM_000489.4:c.6220G=	NP_000480.3:p.Glu2074=
NM_138270.3:c.6106G=	NP_612114.2:p.Glu2036=
XM_005262153.3:c.6217G=	XP_005262210.2:p.Glu2073=
XM_005262154.3:c.6133G=	XP_005262211.2:p.Glu2045=
XM_005262155.3:c.6103G=	XP_005262212.2:p.Glu2035=
XM_005262156.3:c.6055G=	XP_005262213.2:p.Glu2019=
XM_005262157.3:c.6016G=	XP_005262214.2:p.Glu2006=
XM_006724666.2:c.6103G=	XP_006724729.1:p.Glu2035=
XM_006724667.2:c.5941G=	XP_006724730.1:p.Glu1981=
XR_938400.1:n.6562G=
NM_000489.5:c.6220G=	NP_000480.3:p.Glu2074=
XM_005262153.5:c.6217G=	XP_005262210.2:p.Glu2073=
XM_005262154.5:c.6133G=	XP_005262211.2:p.Glu2045=
XM_005262155.4:c.6103G=	XP_005262212.2:p.Glu2035=
XM_005262156.4:c.6055G=	XP_005262213.2:p.Glu2019=
XM_005262157.5:c.6016G=	XP_005262214.2:p.Glu2006=
XM_006724666.4:c.6103G=	XP_006724729.1:p.Glu2035=
XM_006724667.3:c.5941G=	XP_006724730.1:p.Glu1981=
XM_017029601.2:c.6130G=	XP_016885090.1:p.Glu2044=
XM_017029602.1:c.6100G=	XP_016885091.1:p.Glu2034=
XM_017029603.1:c.6052G=	XP_016885092.1:p.Glu2018=
XM_017029604.2:c.6019G=	XP_016885093.1:p.Glu2007=
XM_017029605.1:c.6016G=	XP_016885094.1:p.Glu2006=
XM_017029606.2:c.5989G=	XP_016885095.1:p.Glu1997=
XM_017029607.2:c.5986G=	XP_016885096.1:p.Glu1996=
XM_017029608.2:c.5938G=	XP_016885097.1:p.Glu1980=
XM_017029609.1:c.5902G=	XP_016885098.1:p.Glu1968=
XM_017029610.1:c.5899G=	XP_016885099.1:p.Glu1967=
XM_017029611.1:c.5854G=	XP_016885100.1:p.Glu1952=
XR_001755700.2:n.6519G=
NM_138270.4:c.6106G=	NP_612114.2:p.Glu2036=
NM_000489.6:c.6220G= MANE Select	NP_000480.3:p.Glu2074=
NM_138270.5:c.6106G=	NP_612114.2:p.Glu2036=