Canonical Allele Identifier: CA2694140416

Gene: ATRX

Linked Data

• gnomAD v4: X-77574492-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574493del , CM000685.2:g.77574493del	GRCh38
NC_000023.10:g.76829958del , CM000685.1:g.76829958del	GRCh37
NC_000023.9:g.76716614del	NCBI36
NG_008838.2:g.216729del
NG_008838.3:g.216777del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6218-135del MANE Select	ENSP00000362441.4:n.6218-135del
ENST00000636152.1:n.53-135del
ENST00000675732.1:c.1316-135del	ENSP00000502598.1:n.1316-135del
ENST00000373344.9:c.6218-135del	ENSP00000362441.4:n.6218-135del
ENST00000395603.7:c.6104-135del	ENSP00000378967.3:n.6104-135del
ENST00000480283.5:c.*5846-135del	ENSP00000480196.1:n.*5846-135del
ENST00000623316.1:c.702-135del
ENST00000623706.3:n.3288-135del
NM_000489.4:c.6218-135del	NP_000480.3:n.6218-135del
NM_138270.3:c.6104-135del	NP_612114.2:n.6104-135del
XM_005262153.3:c.6215-135del	XP_005262210.2:n.6215-135del
XM_005262154.3:c.6131-135del	XP_005262211.2:n.6131-135del
XM_005262155.3:c.6101-135del	XP_005262212.2:n.6101-135del
XM_005262156.3:c.6053-135del	XP_005262213.2:n.6053-135del
XM_005262157.3:c.6014-135del	XP_005262214.2:n.6014-135del
XM_006724666.2:c.6101-135del	XP_006724729.1:n.6101-135del
XM_006724667.2:c.5939-135del	XP_006724730.1:n.5939-135del
XR_938400.1:n.6560-135del
NM_000489.5:c.6218-135del	NP_000480.3:n.6218-135del
XM_005262153.5:c.6215-135del	XP_005262210.2:n.6215-135del
XM_005262154.5:c.6131-135del	XP_005262211.2:n.6131-135del
XM_005262155.4:c.6101-135del	XP_005262212.2:n.6101-135del
XM_005262156.4:c.6053-135del	XP_005262213.2:n.6053-135del
XM_005262157.5:c.6014-135del	XP_005262214.2:n.6014-135del
XM_006724666.4:c.6101-135del	XP_006724729.1:n.6101-135del
XM_006724667.3:c.5939-135del	XP_006724730.1:n.5939-135del
XM_017029601.2:c.6128-135del	XP_016885090.1:n.6128-135del
XM_017029602.1:c.6098-135del	XP_016885091.1:n.6098-135del
XM_017029603.1:c.6050-135del	XP_016885092.1:n.6050-135del
XM_017029604.2:c.6017-135del	XP_016885093.1:n.6017-135del
XM_017029605.1:c.6014-135del	XP_016885094.1:n.6014-135del
XM_017029606.2:c.5987-135del	XP_016885095.1:n.5987-135del
XM_017029607.2:c.5984-135del	XP_016885096.1:n.5984-135del
XM_017029608.2:c.5936-135del	XP_016885097.1:n.5936-135del
XM_017029609.1:c.5900-135del	XP_016885098.1:n.5900-135del
XM_017029610.1:c.5897-135del	XP_016885099.1:n.5897-135del
XM_017029611.1:c.5852-135del	XP_016885100.1:n.5852-135del
XR_001755700.2:n.6517-135del
NM_138270.4:c.6104-135del	NP_612114.2:n.6104-135del
NM_000489.6:c.6218-135del MANE Select	NP_000480.3:n.6218-135del
NM_138270.5:c.6104-135del	NP_612114.2:n.6104-135del