Canonical Allele Identifier: CA2694142567
Gene: ATRX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652374_77652379del , CM000685.2:g.77652374_77652379del GRCh38
NC_000023.10:g.76907864_76907869del , CM000685.1:g.76907864_76907869del GRCh37
NC_000023.9:g.76794520_76794525del NCBI36
NG_008838.2:g.138845_138850del
NG_008838.3:g.138893_138898del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4318-24_4318-19del MANE Select ENSP00000362441.4:n.4318-24_4318-19del
ENST00000373344.9:c.4318-24_4318-19del ENSP00000362441.4:n.4318-24_4318-19del
ENST00000395603.7:c.4204-24_4204-19del ENSP00000378967.3:n.4204-24_4204-19del
ENST00000480283.5:c.*3946-24_*3946-19del ENSP00000480196.1:n.*3946-24_*3946-19del
NM_000489.4:c.4318-24_4318-19del NP_000480.3:n.4318-24_4318-19del
NM_138270.3:c.4204-24_4204-19del NP_612114.2:n.4204-24_4204-19del
XM_005262153.3:c.4315-24_4315-19del XP_005262210.2:n.4315-24_4315-19del
XM_005262154.3:c.4231-24_4231-19del XP_005262211.2:n.4231-24_4231-19del
XM_005262155.3:c.4201-24_4201-19del XP_005262212.2:n.4201-24_4201-19del
XM_005262156.3:c.4153-24_4153-19del XP_005262213.2:n.4153-24_4153-19del
XM_005262157.3:c.4114-24_4114-19del XP_005262214.2:n.4114-24_4114-19del
XM_006724666.2:c.4201-24_4201-19del XP_006724729.1:n.4201-24_4201-19del
XM_006724667.2:c.4039-24_4039-19del XP_006724730.1:n.4039-24_4039-19del
XM_006724668.2:c.4318-24_4318-19del XP_006724731.1:n.4318-24_4318-19del
XR_938400.1:n.4586-24_4586-19del
NM_000489.5:c.4318-24_4318-19del NP_000480.3:n.4318-24_4318-19del
XM_005262153.5:c.4315-24_4315-19del XP_005262210.2:n.4315-24_4315-19del
XM_005262154.5:c.4231-24_4231-19del XP_005262211.2:n.4231-24_4231-19del
XM_005262155.4:c.4201-24_4201-19del XP_005262212.2:n.4201-24_4201-19del
XM_005262156.4:c.4153-24_4153-19del XP_005262213.2:n.4153-24_4153-19del
XM_005262157.5:c.4114-24_4114-19del XP_005262214.2:n.4114-24_4114-19del
XM_006724666.4:c.4201-24_4201-19del XP_006724729.1:n.4201-24_4201-19del
XM_006724667.3:c.4039-24_4039-19del XP_006724730.1:n.4039-24_4039-19del
XM_006724668.3:c.4318-24_4318-19del XP_006724731.1:n.4318-24_4318-19del
XM_017029601.2:c.4228-24_4228-19del XP_016885090.1:n.4228-24_4228-19del
XM_017029602.1:c.4198-24_4198-19del XP_016885091.1:n.4198-24_4198-19del
XM_017029603.1:c.4150-24_4150-19del XP_016885092.1:n.4150-24_4150-19del
XM_017029604.2:c.4117-24_4117-19del XP_016885093.1:n.4117-24_4117-19del
XM_017029605.1:c.4114-24_4114-19del XP_016885094.1:n.4114-24_4114-19del
XM_017029606.2:c.4087-24_4087-19del XP_016885095.1:n.4087-24_4087-19del
XM_017029607.2:c.4084-24_4084-19del XP_016885096.1:n.4084-24_4084-19del
XM_017029608.2:c.4036-24_4036-19del XP_016885097.1:n.4036-24_4036-19del
XM_017029609.1:c.4000-24_4000-19del XP_016885098.1:n.4000-24_4000-19del
XM_017029610.1:c.3997-24_3997-19del XP_016885099.1:n.3997-24_3997-19del
XM_017029611.1:c.3952-24_3952-19del XP_016885100.1:n.3952-24_3952-19del
XR_001755700.2:n.4543-24_4543-19del
NM_138270.4:c.4204-24_4204-19del NP_612114.2:n.4204-24_4204-19del
NM_000489.6:c.4318-24_4318-19del MANE Select NP_000480.3:n.4318-24_4318-19del
NM_138270.5:c.4204-24_4204-19del NP_612114.2:n.4204-24_4204-19del