Canonical Allele Identifier: CA2694142566

Gene: ATRX

Linked Data

• gnomAD v4: X-77652368-CAATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652370_77652373del , CM000685.2:g.77652370_77652373del	GRCh38
NC_000023.10:g.76907860_76907863del , CM000685.1:g.76907860_76907863del	GRCh37
NC_000023.9:g.76794516_76794519del	NCBI36
NG_008838.2:g.138850_138853del
NG_008838.3:g.138898_138901del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4318-19_4318-16del MANE Select	ENSP00000362441.4:n.4318-19_4318-16del
ENST00000373344.9:c.4318-19_4318-16del	ENSP00000362441.4:n.4318-19_4318-16del
ENST00000395603.7:c.4204-19_4204-16del	ENSP00000378967.3:n.4204-19_4204-16del
ENST00000480283.5:c.*3946-19_*3946-16del	ENSP00000480196.1:n.*3946-19_*3946-16del
NM_000489.4:c.4318-19_4318-16del	NP_000480.3:n.4318-19_4318-16del
NM_138270.3:c.4204-19_4204-16del	NP_612114.2:n.4204-19_4204-16del
XM_005262153.3:c.4315-19_4315-16del	XP_005262210.2:n.4315-19_4315-16del
XM_005262154.3:c.4231-19_4231-16del	XP_005262211.2:n.4231-19_4231-16del
XM_005262155.3:c.4201-19_4201-16del	XP_005262212.2:n.4201-19_4201-16del
XM_005262156.3:c.4153-19_4153-16del	XP_005262213.2:n.4153-19_4153-16del
XM_005262157.3:c.4114-19_4114-16del	XP_005262214.2:n.4114-19_4114-16del
XM_006724666.2:c.4201-19_4201-16del	XP_006724729.1:n.4201-19_4201-16del
XM_006724667.2:c.4039-19_4039-16del	XP_006724730.1:n.4039-19_4039-16del
XM_006724668.2:c.4318-19_4318-16del	XP_006724731.1:n.4318-19_4318-16del
XR_938400.1:n.4586-19_4586-16del
NM_000489.5:c.4318-19_4318-16del	NP_000480.3:n.4318-19_4318-16del
XM_005262153.5:c.4315-19_4315-16del	XP_005262210.2:n.4315-19_4315-16del
XM_005262154.5:c.4231-19_4231-16del	XP_005262211.2:n.4231-19_4231-16del
XM_005262155.4:c.4201-19_4201-16del	XP_005262212.2:n.4201-19_4201-16del
XM_005262156.4:c.4153-19_4153-16del	XP_005262213.2:n.4153-19_4153-16del
XM_005262157.5:c.4114-19_4114-16del	XP_005262214.2:n.4114-19_4114-16del
XM_006724666.4:c.4201-19_4201-16del	XP_006724729.1:n.4201-19_4201-16del
XM_006724667.3:c.4039-19_4039-16del	XP_006724730.1:n.4039-19_4039-16del
XM_006724668.3:c.4318-19_4318-16del	XP_006724731.1:n.4318-19_4318-16del
XM_017029601.2:c.4228-19_4228-16del	XP_016885090.1:n.4228-19_4228-16del
XM_017029602.1:c.4198-19_4198-16del	XP_016885091.1:n.4198-19_4198-16del
XM_017029603.1:c.4150-19_4150-16del	XP_016885092.1:n.4150-19_4150-16del
XM_017029604.2:c.4117-19_4117-16del	XP_016885093.1:n.4117-19_4117-16del
XM_017029605.1:c.4114-19_4114-16del	XP_016885094.1:n.4114-19_4114-16del
XM_017029606.2:c.4087-19_4087-16del	XP_016885095.1:n.4087-19_4087-16del
XM_017029607.2:c.4084-19_4084-16del	XP_016885096.1:n.4084-19_4084-16del
XM_017029608.2:c.4036-19_4036-16del	XP_016885097.1:n.4036-19_4036-16del
XM_017029609.1:c.4000-19_4000-16del	XP_016885098.1:n.4000-19_4000-16del
XM_017029610.1:c.3997-19_3997-16del	XP_016885099.1:n.3997-19_3997-16del
XM_017029611.1:c.3952-19_3952-16del	XP_016885100.1:n.3952-19_3952-16del
XR_001755700.2:n.4543-19_4543-16del
NM_138270.4:c.4204-19_4204-16del	NP_612114.2:n.4204-19_4204-16del
NM_000489.6:c.4318-19_4318-16del MANE Select	NP_000480.3:n.4318-19_4318-16del
NM_138270.5:c.4204-19_4204-16del	NP_612114.2:n.4204-19_4204-16del