Canonical Allele Identifier: CA2438976902

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652300_77652309delinsCTCCTCCTCT , CM000685.2:g.77652300_77652309delinsCTCCTCCTCT	GRCh38
NC_000023.10:g.76907790_76907799delinsCTCCTCCTCT , CM000685.1:g.76907790_76907799delinsCTCCTCCTCT	GRCh37
NC_000023.9:g.76794446_76794455delinsCTCCTCCTCT	NCBI36
NG_008838.2:g.138913_138922delinsAGAGGAGGAG
NG_008838.3:g.138961_138970delinsAGAGGAGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4362_4371delinsAGAGGAGGAG MANE Select	ENSP00000362441.4:p.Glu1454=
ENST00000373344.9:c.4362_4371delinsAGAGGAGGAG	ENSP00000362441.4:p.Glu1454=
ENST00000395603.7:c.4248_4257delinsAGAGGAGGAG	ENSP00000378967.3:p.Glu1416=
ENST00000480283.5:c.*3990_*3999delinsAGAGGAGGAG	ENSP00000480196.1:n.*3990_*3999delinsAGAGGAGGAG
NM_000489.4:c.4362_4371delinsAGAGGAGGAG	NP_000480.3:p.Glu1454=
NM_138270.3:c.4248_4257delinsAGAGGAGGAG	NP_612114.2:p.Glu1416=
XM_005262153.3:c.4359_4368delinsAGAGGAGGAG	XP_005262210.2:p.Glu1453=
XM_005262154.3:c.4275_4284delinsAGAGGAGGAG	XP_005262211.2:p.Glu1425=
XM_005262155.3:c.4245_4254delinsAGAGGAGGAG	XP_005262212.2:p.Glu1415=
XM_005262156.3:c.4197_4206delinsAGAGGAGGAG	XP_005262213.2:p.Glu1399=
XM_005262157.3:c.4158_4167delinsAGAGGAGGAG	XP_005262214.2:p.Glu1386=
XM_006724666.2:c.4245_4254delinsAGAGGAGGAG	XP_006724729.1:p.Glu1415=
XM_006724667.2:c.4083_4092delinsAGAGGAGGAG	XP_006724730.1:p.Glu1361=
XM_006724668.2:c.4362_4371delinsAGAGGAGGAG	XP_006724731.1:p.Glu1454=
XR_938400.1:n.4630_4639delinsAGAGGAGGAG
NM_000489.5:c.4362_4371delinsAGAGGAGGAG	NP_000480.3:p.Glu1454=
XM_005262153.5:c.4359_4368delinsAGAGGAGGAG	XP_005262210.2:p.Glu1453=
XM_005262154.5:c.4275_4284delinsAGAGGAGGAG	XP_005262211.2:p.Glu1425=
XM_005262155.4:c.4245_4254delinsAGAGGAGGAG	XP_005262212.2:p.Glu1415=
XM_005262156.4:c.4197_4206delinsAGAGGAGGAG	XP_005262213.2:p.Glu1399=
XM_005262157.5:c.4158_4167delinsAGAGGAGGAG	XP_005262214.2:p.Glu1386=
XM_006724666.4:c.4245_4254delinsAGAGGAGGAG	XP_006724729.1:p.Glu1415=
XM_006724667.3:c.4083_4092delinsAGAGGAGGAG	XP_006724730.1:p.Glu1361=
XM_006724668.3:c.4362_4371delinsAGAGGAGGAG	XP_006724731.1:p.Glu1454=
XM_017029601.2:c.4272_4281delinsAGAGGAGGAG	XP_016885090.1:p.Glu1424=
XM_017029602.1:c.4242_4251delinsAGAGGAGGAG	XP_016885091.1:p.Glu1414=
XM_017029603.1:c.4194_4203delinsAGAGGAGGAG	XP_016885092.1:p.Glu1398=
XM_017029604.2:c.4161_4170delinsAGAGGAGGAG	XP_016885093.1:p.Glu1387=
XM_017029605.1:c.4158_4167delinsAGAGGAGGAG	XP_016885094.1:p.Glu1386=
XM_017029606.2:c.4131_4140delinsAGAGGAGGAG	XP_016885095.1:p.Glu1377=
XM_017029607.2:c.4128_4137delinsAGAGGAGGAG	XP_016885096.1:p.Glu1376=
XM_017029608.2:c.4080_4089delinsAGAGGAGGAG	XP_016885097.1:p.Glu1360=
XM_017029609.1:c.4044_4053delinsAGAGGAGGAG	XP_016885098.1:p.Glu1348=
XM_017029610.1:c.4041_4050delinsAGAGGAGGAG	XP_016885099.1:p.Glu1347=
XM_017029611.1:c.3996_4005delinsAGAGGAGGAG	XP_016885100.1:p.Glu1332=
XR_001755700.2:n.4587_4596delinsAGAGGAGGAG
NM_138270.4:c.4248_4257delinsAGAGGAGGAG	NP_612114.2:p.Glu1416=
NM_000489.6:c.4362_4371delinsAGAGGAGGAG MANE Select	NP_000480.3:p.Glu1454=
NM_138270.5:c.4248_4257delinsAGAGGAGGAG	NP_612114.2:p.Glu1416=