Canonical Allele Identifier: CA2438976971

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652333_77652336delinsCTCT , CM000685.2:g.77652333_77652336delinsCTCT	GRCh38
NC_000023.10:g.76907823_76907826delinsCTCT , CM000685.1:g.76907823_76907826delinsCTCT	GRCh37
NC_000023.9:g.76794479_76794482delinsCTCT	NCBI36
NG_008838.2:g.138886_138889delinsAGAG
NG_008838.3:g.138934_138937delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4335_4338delinsAGAG MANE Select	ENSP00000362441.4:p.Glu1445=
ENST00000373344.9:c.4335_4338delinsAGAG	ENSP00000362441.4:p.Glu1445=
ENST00000395603.7:c.4221_4224delinsAGAG	ENSP00000378967.3:p.Glu1407=
ENST00000480283.5:c.*3963_*3966delinsAGAG	ENSP00000480196.1:n.*3963_*3966delinsAGAG
NM_000489.4:c.4335_4338delinsAGAG	NP_000480.3:p.Glu1445=
NM_138270.3:c.4221_4224delinsAGAG	NP_612114.2:p.Glu1407=
XM_005262153.3:c.4332_4335delinsAGAG	XP_005262210.2:p.Glu1444=
XM_005262154.3:c.4248_4251delinsAGAG	XP_005262211.2:p.Glu1416=
XM_005262155.3:c.4218_4221delinsAGAG	XP_005262212.2:p.Glu1406=
XM_005262156.3:c.4170_4173delinsAGAG	XP_005262213.2:p.Glu1390=
XM_005262157.3:c.4131_4134delinsAGAG	XP_005262214.2:p.Glu1377=
XM_006724666.2:c.4218_4221delinsAGAG	XP_006724729.1:p.Glu1406=
XM_006724667.2:c.4056_4059delinsAGAG	XP_006724730.1:p.Glu1352=
XM_006724668.2:c.4335_4338delinsAGAG	XP_006724731.1:p.Glu1445=
XR_938400.1:n.4603_4606delinsAGAG
NM_000489.5:c.4335_4338delinsAGAG	NP_000480.3:p.Glu1445=
XM_005262153.5:c.4332_4335delinsAGAG	XP_005262210.2:p.Glu1444=
XM_005262154.5:c.4248_4251delinsAGAG	XP_005262211.2:p.Glu1416=
XM_005262155.4:c.4218_4221delinsAGAG	XP_005262212.2:p.Glu1406=
XM_005262156.4:c.4170_4173delinsAGAG	XP_005262213.2:p.Glu1390=
XM_005262157.5:c.4131_4134delinsAGAG	XP_005262214.2:p.Glu1377=
XM_006724666.4:c.4218_4221delinsAGAG	XP_006724729.1:p.Glu1406=
XM_006724667.3:c.4056_4059delinsAGAG	XP_006724730.1:p.Glu1352=
XM_006724668.3:c.4335_4338delinsAGAG	XP_006724731.1:p.Glu1445=
XM_017029601.2:c.4245_4248delinsAGAG	XP_016885090.1:p.Glu1415=
XM_017029602.1:c.4215_4218delinsAGAG	XP_016885091.1:p.Glu1405=
XM_017029603.1:c.4167_4170delinsAGAG	XP_016885092.1:p.Glu1389=
XM_017029604.2:c.4134_4137delinsAGAG	XP_016885093.1:p.Glu1378=
XM_017029605.1:c.4131_4134delinsAGAG	XP_016885094.1:p.Glu1377=
XM_017029606.2:c.4104_4107delinsAGAG	XP_016885095.1:p.Glu1368=
XM_017029607.2:c.4101_4104delinsAGAG	XP_016885096.1:p.Glu1367=
XM_017029608.2:c.4053_4056delinsAGAG	XP_016885097.1:p.Glu1351=
XM_017029609.1:c.4017_4020delinsAGAG	XP_016885098.1:p.Glu1339=
XM_017029610.1:c.4014_4017delinsAGAG	XP_016885099.1:p.Glu1338=
XM_017029611.1:c.3969_3972delinsAGAG	XP_016885100.1:p.Glu1323=
XR_001755700.2:n.4560_4563delinsAGAG
NM_138270.4:c.4221_4224delinsAGAG	NP_612114.2:p.Glu1407=
NM_000489.6:c.4335_4338delinsAGAG MANE Select	NP_000480.3:p.Glu1445=
NM_138270.5:c.4221_4224delinsAGAG	NP_612114.2:p.Glu1407=