Canonical Allele Identifier: CA2438976960

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652327_77652330delinsTTCC , CM000685.2:g.77652327_77652330delinsTTCC	GRCh38
NC_000023.10:g.76907817_76907820delinsTTCC , CM000685.1:g.76907817_76907820delinsTTCC	GRCh37
NC_000023.9:g.76794473_76794476delinsTTCC	NCBI36
NG_008838.2:g.138892_138895delinsGGAA
NG_008838.3:g.138940_138943delinsGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4341_4344delinsGGAA MANE Select	ENSP00000362441.4:p.Glu1447=
ENST00000373344.9:c.4341_4344delinsGGAA	ENSP00000362441.4:p.Glu1447=
ENST00000395603.7:c.4227_4230delinsGGAA	ENSP00000378967.3:p.Glu1409=
ENST00000480283.5:c.*3969_*3972delinsGGAA	ENSP00000480196.1:n.*3969_*3972delinsGGAA
NM_000489.4:c.4341_4344delinsGGAA	NP_000480.3:p.Glu1447=
NM_138270.3:c.4227_4230delinsGGAA	NP_612114.2:p.Glu1409=
XM_005262153.3:c.4338_4341delinsGGAA	XP_005262210.2:p.Glu1446=
XM_005262154.3:c.4254_4257delinsGGAA	XP_005262211.2:p.Glu1418=
XM_005262155.3:c.4224_4227delinsGGAA	XP_005262212.2:p.Glu1408=
XM_005262156.3:c.4176_4179delinsGGAA	XP_005262213.2:p.Glu1392=
XM_005262157.3:c.4137_4140delinsGGAA	XP_005262214.2:p.Glu1379=
XM_006724666.2:c.4224_4227delinsGGAA	XP_006724729.1:p.Glu1408=
XM_006724667.2:c.4062_4065delinsGGAA	XP_006724730.1:p.Glu1354=
XM_006724668.2:c.4341_4344delinsGGAA	XP_006724731.1:p.Glu1447=
XR_938400.1:n.4609_4612delinsGGAA
NM_000489.5:c.4341_4344delinsGGAA	NP_000480.3:p.Glu1447=
XM_005262153.5:c.4338_4341delinsGGAA	XP_005262210.2:p.Glu1446=
XM_005262154.5:c.4254_4257delinsGGAA	XP_005262211.2:p.Glu1418=
XM_005262155.4:c.4224_4227delinsGGAA	XP_005262212.2:p.Glu1408=
XM_005262156.4:c.4176_4179delinsGGAA	XP_005262213.2:p.Glu1392=
XM_005262157.5:c.4137_4140delinsGGAA	XP_005262214.2:p.Glu1379=
XM_006724666.4:c.4224_4227delinsGGAA	XP_006724729.1:p.Glu1408=
XM_006724667.3:c.4062_4065delinsGGAA	XP_006724730.1:p.Glu1354=
XM_006724668.3:c.4341_4344delinsGGAA	XP_006724731.1:p.Glu1447=
XM_017029601.2:c.4251_4254delinsGGAA	XP_016885090.1:p.Glu1417=
XM_017029602.1:c.4221_4224delinsGGAA	XP_016885091.1:p.Glu1407=
XM_017029603.1:c.4173_4176delinsGGAA	XP_016885092.1:p.Glu1391=
XM_017029604.2:c.4140_4143delinsGGAA	XP_016885093.1:p.Glu1380=
XM_017029605.1:c.4137_4140delinsGGAA	XP_016885094.1:p.Glu1379=
XM_017029606.2:c.4110_4113delinsGGAA	XP_016885095.1:p.Glu1370=
XM_017029607.2:c.4107_4110delinsGGAA	XP_016885096.1:p.Glu1369=
XM_017029608.2:c.4059_4062delinsGGAA	XP_016885097.1:p.Glu1353=
XM_017029609.1:c.4023_4026delinsGGAA	XP_016885098.1:p.Glu1341=
XM_017029610.1:c.4020_4023delinsGGAA	XP_016885099.1:p.Glu1340=
XM_017029611.1:c.3975_3978delinsGGAA	XP_016885100.1:p.Glu1325=
XR_001755700.2:n.4566_4569delinsGGAA
NM_138270.4:c.4227_4230delinsGGAA	NP_612114.2:p.Glu1409=
NM_000489.6:c.4341_4344delinsGGAA MANE Select	NP_000480.3:p.Glu1447=
NM_138270.5:c.4227_4230delinsGGAA	NP_612114.2:p.Glu1409=