Canonical Allele Identifier: CA2438977011
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652387_77652389delinsCAA , CM000685.2:g.77652387_77652389delinsCAA GRCh38
NC_000023.10:g.76907877_76907879delinsCAA , CM000685.1:g.76907877_76907879delinsCAA GRCh37
NC_000023.9:g.76794533_76794535delinsCAA NCBI36
NG_008838.2:g.138833_138835delinsTTG
NG_008838.3:g.138881_138883delinsTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4318-36_4318-34delinsTTG MANE Select ENSP00000362441.4:n.4318-36_4318-34delinsTTG
ENST00000373344.9:c.4318-36_4318-34delinsTTG ENSP00000362441.4:n.4318-36_4318-34delinsTTG
ENST00000395603.7:c.4204-36_4204-34delinsTTG ENSP00000378967.3:n.4204-36_4204-34delinsTTG
ENST00000480283.5:c.*3946-36_*3946-34delinsTTG ENSP00000480196.1:n.*3946-36_*3946-34delinsTTG
NM_000489.4:c.4318-36_4318-34delinsTTG NP_000480.3:n.4318-36_4318-34delinsTTG
NM_138270.3:c.4204-36_4204-34delinsTTG NP_612114.2:n.4204-36_4204-34delinsTTG
XM_005262153.3:c.4315-36_4315-34delinsTTG XP_005262210.2:n.4315-36_4315-34delinsTTG
XM_005262154.3:c.4231-36_4231-34delinsTTG XP_005262211.2:n.4231-36_4231-34delinsTTG
XM_005262155.3:c.4201-36_4201-34delinsTTG XP_005262212.2:n.4201-36_4201-34delinsTTG
XM_005262156.3:c.4153-36_4153-34delinsTTG XP_005262213.2:n.4153-36_4153-34delinsTTG
XM_005262157.3:c.4114-36_4114-34delinsTTG XP_005262214.2:n.4114-36_4114-34delinsTTG
XM_006724666.2:c.4201-36_4201-34delinsTTG XP_006724729.1:n.4201-36_4201-34delinsTTG
XM_006724667.2:c.4039-36_4039-34delinsTTG XP_006724730.1:n.4039-36_4039-34delinsTTG
XM_006724668.2:c.4318-36_4318-34delinsTTG XP_006724731.1:n.4318-36_4318-34delinsTTG
XR_938400.1:n.4586-36_4586-34delinsTTG
NM_000489.5:c.4318-36_4318-34delinsTTG NP_000480.3:n.4318-36_4318-34delinsTTG
XM_005262153.5:c.4315-36_4315-34delinsTTG XP_005262210.2:n.4315-36_4315-34delinsTTG
XM_005262154.5:c.4231-36_4231-34delinsTTG XP_005262211.2:n.4231-36_4231-34delinsTTG
XM_005262155.4:c.4201-36_4201-34delinsTTG XP_005262212.2:n.4201-36_4201-34delinsTTG
XM_005262156.4:c.4153-36_4153-34delinsTTG XP_005262213.2:n.4153-36_4153-34delinsTTG
XM_005262157.5:c.4114-36_4114-34delinsTTG XP_005262214.2:n.4114-36_4114-34delinsTTG
XM_006724666.4:c.4201-36_4201-34delinsTTG XP_006724729.1:n.4201-36_4201-34delinsTTG
XM_006724667.3:c.4039-36_4039-34delinsTTG XP_006724730.1:n.4039-36_4039-34delinsTTG
XM_006724668.3:c.4318-36_4318-34delinsTTG XP_006724731.1:n.4318-36_4318-34delinsTTG
XM_017029601.2:c.4228-36_4228-34delinsTTG XP_016885090.1:n.4228-36_4228-34delinsTTG
XM_017029602.1:c.4198-36_4198-34delinsTTG XP_016885091.1:n.4198-36_4198-34delinsTTG
XM_017029603.1:c.4150-36_4150-34delinsTTG XP_016885092.1:n.4150-36_4150-34delinsTTG
XM_017029604.2:c.4117-36_4117-34delinsTTG XP_016885093.1:n.4117-36_4117-34delinsTTG
XM_017029605.1:c.4114-36_4114-34delinsTTG XP_016885094.1:n.4114-36_4114-34delinsTTG
XM_017029606.2:c.4087-36_4087-34delinsTTG XP_016885095.1:n.4087-36_4087-34delinsTTG
XM_017029607.2:c.4084-36_4084-34delinsTTG XP_016885096.1:n.4084-36_4084-34delinsTTG
XM_017029608.2:c.4036-36_4036-34delinsTTG XP_016885097.1:n.4036-36_4036-34delinsTTG
XM_017029609.1:c.4000-36_4000-34delinsTTG XP_016885098.1:n.4000-36_4000-34delinsTTG
XM_017029610.1:c.3997-36_3997-34delinsTTG XP_016885099.1:n.3997-36_3997-34delinsTTG
XM_017029611.1:c.3952-36_3952-34delinsTTG XP_016885100.1:n.3952-36_3952-34delinsTTG
XR_001755700.2:n.4543-36_4543-34delinsTTG
NM_138270.4:c.4204-36_4204-34delinsTTG NP_612114.2:n.4204-36_4204-34delinsTTG
NM_000489.6:c.4318-36_4318-34delinsTTG MANE Select NP_000480.3:n.4318-36_4318-34delinsTTG
NM_138270.5:c.4204-36_4204-34delinsTTG NP_612114.2:n.4204-36_4204-34delinsTTG