Canonical Allele Identifier: CA2438976857

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652279_77652282delinsTTCC , CM000685.2:g.77652279_77652282delinsTTCC	GRCh38
NC_000023.10:g.76907769_76907772delinsTTCC , CM000685.1:g.76907769_76907772delinsTTCC	GRCh37
NC_000023.9:g.76794425_76794428delinsTTCC	NCBI36
NG_008838.2:g.138940_138943delinsGGAA
NG_008838.3:g.138988_138991delinsGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4389_4392delinsGGAA MANE Select	ENSP00000362441.4:p.Glu1463=
ENST00000373344.9:c.4389_4392delinsGGAA	ENSP00000362441.4:p.Glu1463=
ENST00000395603.7:c.4275_4278delinsGGAA	ENSP00000378967.3:p.Glu1425=
ENST00000480283.5:c.*4017_*4020delinsGGAA	ENSP00000480196.1:n.*4017_*4020delinsGGAA
NM_000489.4:c.4389_4392delinsGGAA	NP_000480.3:p.Glu1463=
NM_138270.3:c.4275_4278delinsGGAA	NP_612114.2:p.Glu1425=
XM_005262153.3:c.4386_4389delinsGGAA	XP_005262210.2:p.Glu1462=
XM_005262154.3:c.4302_4305delinsGGAA	XP_005262211.2:p.Glu1434=
XM_005262155.3:c.4272_4275delinsGGAA	XP_005262212.2:p.Glu1424=
XM_005262156.3:c.4224_4227delinsGGAA	XP_005262213.2:p.Glu1408=
XM_005262157.3:c.4185_4188delinsGGAA	XP_005262214.2:p.Glu1395=
XM_006724666.2:c.4272_4275delinsGGAA	XP_006724729.1:p.Glu1424=
XM_006724667.2:c.4110_4113delinsGGAA	XP_006724730.1:p.Glu1370=
XM_006724668.2:c.4389_4392delinsGGAA	XP_006724731.1:p.Glu1463=
XR_938400.1:n.4657_4660delinsGGAA
NM_000489.5:c.4389_4392delinsGGAA	NP_000480.3:p.Glu1463=
XM_005262153.5:c.4386_4389delinsGGAA	XP_005262210.2:p.Glu1462=
XM_005262154.5:c.4302_4305delinsGGAA	XP_005262211.2:p.Glu1434=
XM_005262155.4:c.4272_4275delinsGGAA	XP_005262212.2:p.Glu1424=
XM_005262156.4:c.4224_4227delinsGGAA	XP_005262213.2:p.Glu1408=
XM_005262157.5:c.4185_4188delinsGGAA	XP_005262214.2:p.Glu1395=
XM_006724666.4:c.4272_4275delinsGGAA	XP_006724729.1:p.Glu1424=
XM_006724667.3:c.4110_4113delinsGGAA	XP_006724730.1:p.Glu1370=
XM_006724668.3:c.4389_4392delinsGGAA	XP_006724731.1:p.Glu1463=
XM_017029601.2:c.4299_4302delinsGGAA	XP_016885090.1:p.Glu1433=
XM_017029602.1:c.4269_4272delinsGGAA	XP_016885091.1:p.Glu1423=
XM_017029603.1:c.4221_4224delinsGGAA	XP_016885092.1:p.Glu1407=
XM_017029604.2:c.4188_4191delinsGGAA	XP_016885093.1:p.Glu1396=
XM_017029605.1:c.4185_4188delinsGGAA	XP_016885094.1:p.Glu1395=
XM_017029606.2:c.4158_4161delinsGGAA	XP_016885095.1:p.Glu1386=
XM_017029607.2:c.4155_4158delinsGGAA	XP_016885096.1:p.Glu1385=
XM_017029608.2:c.4107_4110delinsGGAA	XP_016885097.1:p.Glu1369=
XM_017029609.1:c.4071_4074delinsGGAA	XP_016885098.1:p.Glu1357=
XM_017029610.1:c.4068_4071delinsGGAA	XP_016885099.1:p.Glu1356=
XM_017029611.1:c.4023_4026delinsGGAA	XP_016885100.1:p.Glu1341=
XR_001755700.2:n.4614_4617delinsGGAA
NM_138270.4:c.4275_4278delinsGGAA	NP_612114.2:p.Glu1425=
NM_000489.6:c.4389_4392delinsGGAA MANE Select	NP_000480.3:p.Glu1463=
NM_138270.5:c.4275_4278delinsGGAA	NP_612114.2:p.Glu1425=