Canonical Allele Identifier: CA2438976942

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652316T= , CM000685.2:g.77652316T=	GRCh38
NC_000023.10:g.76907806T= , CM000685.1:g.76907806T=	GRCh37
NC_000023.9:g.76794462T=	NCBI36
NG_008838.2:g.138906A=
NG_008838.3:g.138954A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4355A= MANE Select	ENSP00000362441.4:p.Glu1452=
ENST00000373344.9:c.4355A=	ENSP00000362441.4:p.Glu1452=
ENST00000395603.7:c.4241A=	ENSP00000378967.3:p.Glu1414=
ENST00000480283.5:c.*3983A=	ENSP00000480196.1:n.*3983A=
NM_000489.4:c.4355A=	NP_000480.3:p.Glu1452=
NM_138270.3:c.4241A=	NP_612114.2:p.Glu1414=
XM_005262153.3:c.4352A=	XP_005262210.2:p.Glu1451=
XM_005262154.3:c.4268A=	XP_005262211.2:p.Glu1423=
XM_005262155.3:c.4238A=	XP_005262212.2:p.Glu1413=
XM_005262156.3:c.4190A=	XP_005262213.2:p.Glu1397=
XM_005262157.3:c.4151A=	XP_005262214.2:p.Glu1384=
XM_006724666.2:c.4238A=	XP_006724729.1:p.Glu1413=
XM_006724667.2:c.4076A=	XP_006724730.1:p.Glu1359=
XM_006724668.2:c.4355A=	XP_006724731.1:p.Glu1452=
XR_938400.1:n.4623A=
NM_000489.5:c.4355A=	NP_000480.3:p.Glu1452=
XM_005262153.5:c.4352A=	XP_005262210.2:p.Glu1451=
XM_005262154.5:c.4268A=	XP_005262211.2:p.Glu1423=
XM_005262155.4:c.4238A=	XP_005262212.2:p.Glu1413=
XM_005262156.4:c.4190A=	XP_005262213.2:p.Glu1397=
XM_005262157.5:c.4151A=	XP_005262214.2:p.Glu1384=
XM_006724666.4:c.4238A=	XP_006724729.1:p.Glu1413=
XM_006724667.3:c.4076A=	XP_006724730.1:p.Glu1359=
XM_006724668.3:c.4355A=	XP_006724731.1:p.Glu1452=
XM_017029601.2:c.4265A=	XP_016885090.1:p.Glu1422=
XM_017029602.1:c.4235A=	XP_016885091.1:p.Glu1412=
XM_017029603.1:c.4187A=	XP_016885092.1:p.Glu1396=
XM_017029604.2:c.4154A=	XP_016885093.1:p.Glu1385=
XM_017029605.1:c.4151A=	XP_016885094.1:p.Glu1384=
XM_017029606.2:c.4124A=	XP_016885095.1:p.Glu1375=
XM_017029607.2:c.4121A=	XP_016885096.1:p.Glu1374=
XM_017029608.2:c.4073A=	XP_016885097.1:p.Glu1358=
XM_017029609.1:c.4037A=	XP_016885098.1:p.Glu1346=
XM_017029610.1:c.4034A=	XP_016885099.1:p.Glu1345=
XM_017029611.1:c.3989A=	XP_016885100.1:p.Glu1330=
XR_001755700.2:n.4580A=
NM_138270.4:c.4241A=	NP_612114.2:p.Glu1414=
NM_000489.6:c.4355A= MANE Select	NP_000480.3:p.Glu1452=
NM_138270.5:c.4241A=	NP_612114.2:p.Glu1414=