Canonical Allele Identifier: CA2438976874

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652291_77652297delinsTTCCTCC , CM000685.2:g.77652291_77652297delinsTTCCTCC	GRCh38
NC_000023.10:g.76907781_76907787delinsTTCCTCC , CM000685.1:g.76907781_76907787delinsTTCCTCC	GRCh37
NC_000023.9:g.76794437_76794443delinsTTCCTCC	NCBI36
NG_008838.2:g.138925_138931delinsGGAGGAA
NG_008838.3:g.138973_138979delinsGGAGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4374_4380delinsGGAGGAA MANE Select	ENSP00000362441.4:p.Glu1458=
ENST00000373344.9:c.4374_4380delinsGGAGGAA	ENSP00000362441.4:p.Glu1458=
ENST00000395603.7:c.4260_4266delinsGGAGGAA	ENSP00000378967.3:p.Glu1420=
ENST00000480283.5:c.*4002_*4008delinsGGAGGAA	ENSP00000480196.1:n.*4002_*4008delinsGGAGGAA
NM_000489.4:c.4374_4380delinsGGAGGAA	NP_000480.3:p.Glu1458=
NM_138270.3:c.4260_4266delinsGGAGGAA	NP_612114.2:p.Glu1420=
XM_005262153.3:c.4371_4377delinsGGAGGAA	XP_005262210.2:p.Glu1457=
XM_005262154.3:c.4287_4293delinsGGAGGAA	XP_005262211.2:p.Glu1429=
XM_005262155.3:c.4257_4263delinsGGAGGAA	XP_005262212.2:p.Glu1419=
XM_005262156.3:c.4209_4215delinsGGAGGAA	XP_005262213.2:p.Glu1403=
XM_005262157.3:c.4170_4176delinsGGAGGAA	XP_005262214.2:p.Glu1390=
XM_006724666.2:c.4257_4263delinsGGAGGAA	XP_006724729.1:p.Glu1419=
XM_006724667.2:c.4095_4101delinsGGAGGAA	XP_006724730.1:p.Glu1365=
XM_006724668.2:c.4374_4380delinsGGAGGAA	XP_006724731.1:p.Glu1458=
XR_938400.1:n.4642_4648delinsGGAGGAA
NM_000489.5:c.4374_4380delinsGGAGGAA	NP_000480.3:p.Glu1458=
XM_005262153.5:c.4371_4377delinsGGAGGAA	XP_005262210.2:p.Glu1457=
XM_005262154.5:c.4287_4293delinsGGAGGAA	XP_005262211.2:p.Glu1429=
XM_005262155.4:c.4257_4263delinsGGAGGAA	XP_005262212.2:p.Glu1419=
XM_005262156.4:c.4209_4215delinsGGAGGAA	XP_005262213.2:p.Glu1403=
XM_005262157.5:c.4170_4176delinsGGAGGAA	XP_005262214.2:p.Glu1390=
XM_006724666.4:c.4257_4263delinsGGAGGAA	XP_006724729.1:p.Glu1419=
XM_006724667.3:c.4095_4101delinsGGAGGAA	XP_006724730.1:p.Glu1365=
XM_006724668.3:c.4374_4380delinsGGAGGAA	XP_006724731.1:p.Glu1458=
XM_017029601.2:c.4284_4290delinsGGAGGAA	XP_016885090.1:p.Glu1428=
XM_017029602.1:c.4254_4260delinsGGAGGAA	XP_016885091.1:p.Glu1418=
XM_017029603.1:c.4206_4212delinsGGAGGAA	XP_016885092.1:p.Glu1402=
XM_017029604.2:c.4173_4179delinsGGAGGAA	XP_016885093.1:p.Glu1391=
XM_017029605.1:c.4170_4176delinsGGAGGAA	XP_016885094.1:p.Glu1390=
XM_017029606.2:c.4143_4149delinsGGAGGAA	XP_016885095.1:p.Glu1381=
XM_017029607.2:c.4140_4146delinsGGAGGAA	XP_016885096.1:p.Glu1380=
XM_017029608.2:c.4092_4098delinsGGAGGAA	XP_016885097.1:p.Glu1364=
XM_017029609.1:c.4056_4062delinsGGAGGAA	XP_016885098.1:p.Glu1352=
XM_017029610.1:c.4053_4059delinsGGAGGAA	XP_016885099.1:p.Glu1351=
XM_017029611.1:c.4008_4014delinsGGAGGAA	XP_016885100.1:p.Glu1336=
XR_001755700.2:n.4599_4605delinsGGAGGAA
NM_138270.4:c.4260_4266delinsGGAGGAA	NP_612114.2:p.Glu1420=
NM_000489.6:c.4374_4380delinsGGAGGAA MANE Select	NP_000480.3:p.Glu1458=
NM_138270.5:c.4260_4266delinsGGAGGAA	NP_612114.2:p.Glu1420=