Canonical Allele Identifier: CA2579649163

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652324_77652341del , CM000685.2:g.77652324_77652341del	GRCh38
NC_000023.10:g.76907814_76907831del , CM000685.1:g.76907814_76907831del	GRCh37
NC_000023.9:g.76794470_76794487del	NCBI36
NG_008838.2:g.138886_138903del
NG_008838.3:g.138934_138951del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4335_4352del MANE Select	ENSP00000362441.4:p.Glu1446_Glu1451del
ENST00000373344.9:c.4335_4352del	ENSP00000362441.4:p.Glu1446_Glu1451del
ENST00000395603.7:c.4221_4238del	ENSP00000378967.3:p.Glu1408_Glu1413del
ENST00000480283.5:c.*3963_*3980del	ENSP00000480196.1:n.*3963_*3980del
NM_000489.4:c.4335_4352del	NP_000480.3:p.Glu1446_Glu1451del
NM_138270.3:c.4221_4238del	NP_612114.2:p.Glu1408_Glu1413del
XM_005262153.3:c.4332_4349del	XP_005262210.2:p.Glu1445_Glu1450del
XM_005262154.3:c.4248_4265del	XP_005262211.2:p.Glu1417_Glu1422del
XM_005262155.3:c.4218_4235del	XP_005262212.2:p.Glu1407_Glu1412del
XM_005262156.3:c.4170_4187del	XP_005262213.2:p.Glu1391_Glu1396del
XM_005262157.3:c.4131_4148del	XP_005262214.2:p.Glu1378_Glu1383del
XM_006724666.2:c.4218_4235del	XP_006724729.1:p.Glu1407_Glu1412del
XM_006724667.2:c.4056_4073del	XP_006724730.1:p.Glu1353_Glu1358del
XM_006724668.2:c.4335_4352del	XP_006724731.1:p.Glu1446_Glu1451del
XR_938400.1:n.4603_4620del
NM_000489.5:c.4335_4352del	NP_000480.3:p.Glu1446_Glu1451del
XM_005262153.5:c.4332_4349del	XP_005262210.2:p.Glu1445_Glu1450del
XM_005262154.5:c.4248_4265del	XP_005262211.2:p.Glu1417_Glu1422del
XM_005262155.4:c.4218_4235del	XP_005262212.2:p.Glu1407_Glu1412del
XM_005262156.4:c.4170_4187del	XP_005262213.2:p.Glu1391_Glu1396del
XM_005262157.5:c.4131_4148del	XP_005262214.2:p.Glu1378_Glu1383del
XM_006724666.4:c.4218_4235del	XP_006724729.1:p.Glu1407_Glu1412del
XM_006724667.3:c.4056_4073del	XP_006724730.1:p.Glu1353_Glu1358del
XM_006724668.3:c.4335_4352del	XP_006724731.1:p.Glu1446_Glu1451del
XM_017029601.2:c.4245_4262del	XP_016885090.1:p.Glu1416_Glu1421del
XM_017029602.1:c.4215_4232del	XP_016885091.1:p.Glu1406_Glu1411del
XM_017029603.1:c.4167_4184del	XP_016885092.1:p.Glu1390_Glu1395del
XM_017029604.2:c.4134_4151del	XP_016885093.1:p.Glu1379_Glu1384del
XM_017029605.1:c.4131_4148del	XP_016885094.1:p.Glu1378_Glu1383del
XM_017029606.2:c.4104_4121del	XP_016885095.1:p.Glu1369_Glu1374del
XM_017029607.2:c.4101_4118del	XP_016885096.1:p.Glu1368_Glu1373del
XM_017029608.2:c.4053_4070del	XP_016885097.1:p.Glu1352_Glu1357del
XM_017029609.1:c.4017_4034del	XP_016885098.1:p.Glu1340_Glu1345del
XM_017029610.1:c.4014_4031del	XP_016885099.1:p.Glu1339_Glu1344del
XM_017029611.1:c.3969_3986del	XP_016885100.1:p.Glu1324_Glu1329del
XR_001755700.2:n.4560_4577del
NM_138270.4:c.4221_4238del	NP_612114.2:p.Glu1408_Glu1413del
NM_000489.6:c.4335_4352del MANE Select	NP_000480.3:p.Glu1446_Glu1451del
NM_138270.5:c.4221_4238del	NP_612114.2:p.Glu1408_Glu1413del