Canonical Allele Identifier: CA2520886711

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652279_77652296del , CM000685.2:g.77652279_77652296del	GRCh38
NC_000023.10:g.76907769_76907786del , CM000685.1:g.76907769_76907786del	GRCh37
NC_000023.9:g.76794425_76794442del	NCBI36
NG_008838.2:g.138928_138945del
NG_008838.3:g.138976_138993del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4377_4394del MANE Select	ENSP00000362441.4:p.Glu1459_Glu1464del
ENST00000373344.9:c.4377_4394del	ENSP00000362441.4:p.Glu1459_Glu1464del
ENST00000395603.7:c.4263_4280del	ENSP00000378967.3:p.Glu1421_Glu1426del
ENST00000480283.5:c.*4005_*4022del	ENSP00000480196.1:n.*4005_*4022del
NM_000489.4:c.4377_4394del	NP_000480.3:p.Glu1459_Glu1464del
NM_138270.3:c.4263_4280del	NP_612114.2:p.Glu1421_Glu1426del
XM_005262153.3:c.4374_4391del	XP_005262210.2:p.Glu1458_Glu1463del
XM_005262154.3:c.4290_4307del	XP_005262211.2:p.Glu1430_Glu1435del
XM_005262155.3:c.4260_4277del	XP_005262212.2:p.Glu1420_Glu1425del
XM_005262156.3:c.4212_4229del	XP_005262213.2:p.Glu1404_Glu1409del
XM_005262157.3:c.4173_4190del	XP_005262214.2:p.Glu1391_Glu1396del
XM_006724666.2:c.4260_4277del	XP_006724729.1:p.Glu1420_Glu1425del
XM_006724667.2:c.4098_4115del	XP_006724730.1:p.Glu1366_Glu1371del
XM_006724668.2:c.4377_4394del	XP_006724731.1:p.Glu1459_Glu1464del
XR_938400.1:n.4645_4662del
NM_000489.5:c.4377_4394del	NP_000480.3:p.Glu1459_Glu1464del
XM_005262153.5:c.4374_4391del	XP_005262210.2:p.Glu1458_Glu1463del
XM_005262154.5:c.4290_4307del	XP_005262211.2:p.Glu1430_Glu1435del
XM_005262155.4:c.4260_4277del	XP_005262212.2:p.Glu1420_Glu1425del
XM_005262156.4:c.4212_4229del	XP_005262213.2:p.Glu1404_Glu1409del
XM_005262157.5:c.4173_4190del	XP_005262214.2:p.Glu1391_Glu1396del
XM_006724666.4:c.4260_4277del	XP_006724729.1:p.Glu1420_Glu1425del
XM_006724667.3:c.4098_4115del	XP_006724730.1:p.Glu1366_Glu1371del
XM_006724668.3:c.4377_4394del	XP_006724731.1:p.Glu1459_Glu1464del
XM_017029601.2:c.4287_4304del	XP_016885090.1:p.Glu1429_Glu1434del
XM_017029602.1:c.4257_4274del	XP_016885091.1:p.Glu1419_Glu1424del
XM_017029603.1:c.4209_4226del	XP_016885092.1:p.Glu1403_Glu1408del
XM_017029604.2:c.4176_4193del	XP_016885093.1:p.Glu1392_Glu1397del
XM_017029605.1:c.4173_4190del	XP_016885094.1:p.Glu1391_Glu1396del
XM_017029606.2:c.4146_4163del	XP_016885095.1:p.Glu1382_Glu1387del
XM_017029607.2:c.4143_4160del	XP_016885096.1:p.Glu1381_Glu1386del
XM_017029608.2:c.4095_4112del	XP_016885097.1:p.Glu1365_Glu1370del
XM_017029609.1:c.4059_4076del	XP_016885098.1:p.Glu1353_Glu1358del
XM_017029610.1:c.4056_4073del	XP_016885099.1:p.Glu1352_Glu1357del
XM_017029611.1:c.4011_4028del	XP_016885100.1:p.Glu1337_Glu1342del
XR_001755700.2:n.4602_4619del
NM_138270.4:c.4263_4280del	NP_612114.2:p.Glu1421_Glu1426del
NM_000489.6:c.4377_4394del MANE Select	NP_000480.3:p.Glu1459_Glu1464del
NM_138270.5:c.4263_4280del	NP_612114.2:p.Glu1421_Glu1426del