Canonical Allele Identifier: CA2438976860

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652279T= , CM000685.2:g.77652279T=	GRCh38
NC_000023.10:g.76907769T= , CM000685.1:g.76907769T=	GRCh37
NC_000023.9:g.76794425T=	NCBI36
NG_008838.2:g.138943A=
NG_008838.3:g.138991A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4392A= MANE Select	ENSP00000362441.4:p.Glu1464=
ENST00000373344.9:c.4392A=	ENSP00000362441.4:p.Glu1464=
ENST00000395603.7:c.4278A=	ENSP00000378967.3:p.Glu1426=
ENST00000480283.5:c.*4020A=	ENSP00000480196.1:n.*4020A=
NM_000489.4:c.4392A=	NP_000480.3:p.Glu1464=
NM_138270.3:c.4278A=	NP_612114.2:p.Glu1426=
XM_005262153.3:c.4389A=	XP_005262210.2:p.Glu1463=
XM_005262154.3:c.4305A=	XP_005262211.2:p.Glu1435=
XM_005262155.3:c.4275A=	XP_005262212.2:p.Glu1425=
XM_005262156.3:c.4227A=	XP_005262213.2:p.Glu1409=
XM_005262157.3:c.4188A=	XP_005262214.2:p.Glu1396=
XM_006724666.2:c.4275A=	XP_006724729.1:p.Glu1425=
XM_006724667.2:c.4113A=	XP_006724730.1:p.Glu1371=
XM_006724668.2:c.4392A=	XP_006724731.1:p.Glu1464=
XR_938400.1:n.4660A=
NM_000489.5:c.4392A=	NP_000480.3:p.Glu1464=
XM_005262153.5:c.4389A=	XP_005262210.2:p.Glu1463=
XM_005262154.5:c.4305A=	XP_005262211.2:p.Glu1435=
XM_005262155.4:c.4275A=	XP_005262212.2:p.Glu1425=
XM_005262156.4:c.4227A=	XP_005262213.2:p.Glu1409=
XM_005262157.5:c.4188A=	XP_005262214.2:p.Glu1396=
XM_006724666.4:c.4275A=	XP_006724729.1:p.Glu1425=
XM_006724667.3:c.4113A=	XP_006724730.1:p.Glu1371=
XM_006724668.3:c.4392A=	XP_006724731.1:p.Glu1464=
XM_017029601.2:c.4302A=	XP_016885090.1:p.Glu1434=
XM_017029602.1:c.4272A=	XP_016885091.1:p.Glu1424=
XM_017029603.1:c.4224A=	XP_016885092.1:p.Glu1408=
XM_017029604.2:c.4191A=	XP_016885093.1:p.Glu1397=
XM_017029605.1:c.4188A=	XP_016885094.1:p.Glu1396=
XM_017029606.2:c.4161A=	XP_016885095.1:p.Glu1387=
XM_017029607.2:c.4158A=	XP_016885096.1:p.Glu1386=
XM_017029608.2:c.4110A=	XP_016885097.1:p.Glu1370=
XM_017029609.1:c.4074A=	XP_016885098.1:p.Glu1358=
XM_017029610.1:c.4071A=	XP_016885099.1:p.Glu1357=
XM_017029611.1:c.4026A=	XP_016885100.1:p.Glu1342=
XR_001755700.2:n.4617A=
NM_138270.4:c.4278A=	NP_612114.2:p.Glu1426=
NM_000489.6:c.4392A= MANE Select	NP_000480.3:p.Glu1464=
NM_138270.5:c.4278A=	NP_612114.2:p.Glu1426=