Canonical Allele Identifier: CA517471497

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907775_76907776insCT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652285_77652286insCT , CM000685.2:g.77652285_77652286insCT	GRCh38
NC_000023.10:g.76907775_76907776insCT , CM000685.1:g.76907775_76907776insCT	GRCh37
NC_000023.9:g.76794431_76794432insCT	NCBI36
NG_008838.2:g.138936_138937insAG
NG_008838.3:g.138984_138985insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4385_4386insAG MANE Select	ENSP00000362441.4:p.Glu1463GlyfsTer28
ENST00000373344.9:c.4385_4386insAG	ENSP00000362441.4:p.Glu1463GlyfsTer28
ENST00000395603.7:c.4271_4272insAG	ENSP00000378967.3:p.Glu1425GlyfsTer28
ENST00000480283.5:c.*4013_*4014insAG	ENSP00000480196.1:n.*4013_*4014insAG
NM_000489.4:c.4385_4386insAG	NP_000480.3:p.Glu1463GlyfsTer28
NM_138270.3:c.4271_4272insAG	NP_612114.2:p.Glu1425GlyfsTer28
XM_005262153.3:c.4382_4383insAG	XP_005262210.2:p.Glu1462GlyfsTer28
XM_005262154.3:c.4298_4299insAG	XP_005262211.2:p.Glu1434GlyfsTer28
XM_005262155.3:c.4268_4269insAG	XP_005262212.2:p.Glu1424GlyfsTer28
XM_005262156.3:c.4220_4221insAG	XP_005262213.2:p.Glu1408GlyfsTer28
XM_005262157.3:c.4181_4182insAG	XP_005262214.2:p.Glu1395GlyfsTer28
XM_006724666.2:c.4268_4269insAG	XP_006724729.1:p.Glu1424GlyfsTer28
XM_006724667.2:c.4106_4107insAG	XP_006724730.1:p.Glu1370GlyfsTer28
XM_006724668.2:c.4385_4386insAG	XP_006724731.1:p.Glu1463GlyfsTer28
XR_938400.1:n.4653_4654insAG
NM_000489.5:c.4385_4386insAG	NP_000480.3:p.Glu1463GlyfsTer28
XM_005262153.5:c.4382_4383insAG	XP_005262210.2:p.Glu1462GlyfsTer28
XM_005262154.5:c.4298_4299insAG	XP_005262211.2:p.Glu1434GlyfsTer28
XM_005262155.4:c.4268_4269insAG	XP_005262212.2:p.Glu1424GlyfsTer28
XM_005262156.4:c.4220_4221insAG	XP_005262213.2:p.Glu1408GlyfsTer28
XM_005262157.5:c.4181_4182insAG	XP_005262214.2:p.Glu1395GlyfsTer28
XM_006724666.4:c.4268_4269insAG	XP_006724729.1:p.Glu1424GlyfsTer28
XM_006724667.3:c.4106_4107insAG	XP_006724730.1:p.Glu1370GlyfsTer28
XM_006724668.3:c.4385_4386insAG	XP_006724731.1:p.Glu1463GlyfsTer28
XM_017029601.2:c.4295_4296insAG	XP_016885090.1:p.Glu1433GlyfsTer28
XM_017029602.1:c.4265_4266insAG	XP_016885091.1:p.Glu1423GlyfsTer28
XM_017029603.1:c.4217_4218insAG	XP_016885092.1:p.Glu1407GlyfsTer28
XM_017029604.2:c.4184_4185insAG	XP_016885093.1:p.Glu1396GlyfsTer28
XM_017029605.1:c.4181_4182insAG	XP_016885094.1:p.Glu1395GlyfsTer28
XM_017029606.2:c.4154_4155insAG	XP_016885095.1:p.Glu1386GlyfsTer28
XM_017029607.2:c.4151_4152insAG	XP_016885096.1:p.Glu1385GlyfsTer28
XM_017029608.2:c.4103_4104insAG	XP_016885097.1:p.Glu1369GlyfsTer28
XM_017029609.1:c.4067_4068insAG	XP_016885098.1:p.Glu1357GlyfsTer28
XM_017029610.1:c.4064_4065insAG	XP_016885099.1:p.Glu1356GlyfsTer28
XM_017029611.1:c.4019_4020insAG	XP_016885100.1:p.Glu1341GlyfsTer28
XR_001755700.2:n.4610_4611insAG
NM_138270.4:c.4271_4272insAG	NP_612114.2:p.Glu1425GlyfsTer28
NM_000489.6:c.4385_4386insAG MANE Select	NP_000480.3:p.Glu1463GlyfsTer28
NM_138270.5:c.4271_4272insAG	NP_612114.2:p.Glu1425GlyfsTer28