Canonical Allele Identifier: CA2438977069
Gene: ATRX HGNC NCBI

Linked Data

dbSNP Id: rs1603086063
gnomAD v3: X-77652448-G-A
gnomAD v4: X-77652448-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77652448G>A , CM000685.2:g.77652448G>A GRCh38
NC_000023.10:g.76907938G>A , CM000685.1:g.76907938G>A GRCh37
NC_000023.9:g.76794594G>A NCBI36
NG_008838.2:g.138774C>T
NG_008838.3:g.138822C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.4318-95C>T MANE Select ENSP00000362441.4:n.4318-95C>T
ENST00000373344.9:c.4318-95C>T ENSP00000362441.4:n.4318-95C>T
ENST00000395603.7:c.4204-95C>T ENSP00000378967.3:n.4204-95C>T
ENST00000480283.5:c.*3946-95C>T ENSP00000480196.1:n.*3946-95C>T
NM_000489.4:c.4318-95C>T NP_000480.3:n.4318-95C>T
NM_138270.3:c.4204-95C>T NP_612114.2:n.4204-95C>T
XM_005262153.3:c.4315-95C>T XP_005262210.2:n.4315-95C>T
XM_005262154.3:c.4231-95C>T XP_005262211.2:n.4231-95C>T
XM_005262155.3:c.4201-95C>T XP_005262212.2:n.4201-95C>T
XM_005262156.3:c.4153-95C>T XP_005262213.2:n.4153-95C>T
XM_005262157.3:c.4114-95C>T XP_005262214.2:n.4114-95C>T
XM_006724666.2:c.4201-95C>T XP_006724729.1:n.4201-95C>T
XM_006724667.2:c.4039-95C>T XP_006724730.1:n.4039-95C>T
XM_006724668.2:c.4318-95C>T XP_006724731.1:n.4318-95C>T
XR_938400.1:n.4586-95C>T
NM_000489.5:c.4318-95C>T NP_000480.3:n.4318-95C>T
XM_005262153.5:c.4315-95C>T XP_005262210.2:n.4315-95C>T
XM_005262154.5:c.4231-95C>T XP_005262211.2:n.4231-95C>T
XM_005262155.4:c.4201-95C>T XP_005262212.2:n.4201-95C>T
XM_005262156.4:c.4153-95C>T XP_005262213.2:n.4153-95C>T
XM_005262157.5:c.4114-95C>T XP_005262214.2:n.4114-95C>T
XM_006724666.4:c.4201-95C>T XP_006724729.1:n.4201-95C>T
XM_006724667.3:c.4039-95C>T XP_006724730.1:n.4039-95C>T
XM_006724668.3:c.4318-95C>T XP_006724731.1:n.4318-95C>T
XM_017029601.2:c.4228-95C>T XP_016885090.1:n.4228-95C>T
XM_017029602.1:c.4198-95C>T XP_016885091.1:n.4198-95C>T
XM_017029603.1:c.4150-95C>T XP_016885092.1:n.4150-95C>T
XM_017029604.2:c.4117-95C>T XP_016885093.1:n.4117-95C>T
XM_017029605.1:c.4114-95C>T XP_016885094.1:n.4114-95C>T
XM_017029606.2:c.4087-95C>T XP_016885095.1:n.4087-95C>T
XM_017029607.2:c.4084-95C>T XP_016885096.1:n.4084-95C>T
XM_017029608.2:c.4036-95C>T XP_016885097.1:n.4036-95C>T
XM_017029609.1:c.4000-95C>T XP_016885098.1:n.4000-95C>T
XM_017029610.1:c.3997-95C>T XP_016885099.1:n.3997-95C>T
XM_017029611.1:c.3952-95C>T XP_016885100.1:n.3952-95C>T
XR_001755700.2:n.4543-95C>T
NM_138270.4:c.4204-95C>T NP_612114.2:n.4204-95C>T
NM_000489.6:c.4318-95C>T MANE Select NP_000480.3:n.4318-95C>T
NM_138270.5:c.4204-95C>T NP_612114.2:n.4204-95C>T