Canonical Allele Identifier: CA2438976868

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652288C= , CM000685.2:g.77652288C=	GRCh38
NC_000023.10:g.76907778C= , CM000685.1:g.76907778C=	GRCh37
NC_000023.9:g.76794434C=	NCBI36
NG_008838.2:g.138934G=
NG_008838.3:g.138982G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4383G= MANE Select	ENSP00000362441.4:p.Glu1461=
ENST00000373344.9:c.4383G=	ENSP00000362441.4:p.Glu1461=
ENST00000395603.7:c.4269G=	ENSP00000378967.3:p.Glu1423=
ENST00000480283.5:c.*4011G=	ENSP00000480196.1:n.*4011G=
NM_000489.4:c.4383G=	NP_000480.3:p.Glu1461=
NM_138270.3:c.4269G=	NP_612114.2:p.Glu1423=
XM_005262153.3:c.4380G=	XP_005262210.2:p.Glu1460=
XM_005262154.3:c.4296G=	XP_005262211.2:p.Glu1432=
XM_005262155.3:c.4266G=	XP_005262212.2:p.Glu1422=
XM_005262156.3:c.4218G=	XP_005262213.2:p.Glu1406=
XM_005262157.3:c.4179G=	XP_005262214.2:p.Glu1393=
XM_006724666.2:c.4266G=	XP_006724729.1:p.Glu1422=
XM_006724667.2:c.4104G=	XP_006724730.1:p.Glu1368=
XM_006724668.2:c.4383G=	XP_006724731.1:p.Glu1461=
XR_938400.1:n.4651G=
NM_000489.5:c.4383G=	NP_000480.3:p.Glu1461=
XM_005262153.5:c.4380G=	XP_005262210.2:p.Glu1460=
XM_005262154.5:c.4296G=	XP_005262211.2:p.Glu1432=
XM_005262155.4:c.4266G=	XP_005262212.2:p.Glu1422=
XM_005262156.4:c.4218G=	XP_005262213.2:p.Glu1406=
XM_005262157.5:c.4179G=	XP_005262214.2:p.Glu1393=
XM_006724666.4:c.4266G=	XP_006724729.1:p.Glu1422=
XM_006724667.3:c.4104G=	XP_006724730.1:p.Glu1368=
XM_006724668.3:c.4383G=	XP_006724731.1:p.Glu1461=
XM_017029601.2:c.4293G=	XP_016885090.1:p.Glu1431=
XM_017029602.1:c.4263G=	XP_016885091.1:p.Glu1421=
XM_017029603.1:c.4215G=	XP_016885092.1:p.Glu1405=
XM_017029604.2:c.4182G=	XP_016885093.1:p.Glu1394=
XM_017029605.1:c.4179G=	XP_016885094.1:p.Glu1393=
XM_017029606.2:c.4152G=	XP_016885095.1:p.Glu1384=
XM_017029607.2:c.4149G=	XP_016885096.1:p.Glu1383=
XM_017029608.2:c.4101G=	XP_016885097.1:p.Glu1367=
XM_017029609.1:c.4065G=	XP_016885098.1:p.Glu1355=
XM_017029610.1:c.4062G=	XP_016885099.1:p.Glu1354=
XM_017029611.1:c.4017G=	XP_016885100.1:p.Glu1339=
XR_001755700.2:n.4608G=
NM_138270.4:c.4269G=	NP_612114.2:p.Glu1423=
NM_000489.6:c.4383G= MANE Select	NP_000480.3:p.Glu1461=
NM_138270.5:c.4269G=	NP_612114.2:p.Glu1423=