Canonical Allele Identifier: CA2438951480

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574552_77574556delinsAATAG , CM000685.2:g.77574552_77574556delinsAATAG	GRCh38
NC_000023.10:g.76830017_76830021delinsAATAG , CM000685.1:g.76830017_76830021delinsAATAG	GRCh37
NC_000023.9:g.76716673_76716677delinsAATAG	NCBI36
NG_008838.2:g.216666_216670delinsCTATT
NG_008838.3:g.216714_216718delinsCTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6218-198_6218-194delinsCTATT MANE Select	ENSP00000362441.4:n.6218-198_6218-194delinsCTATT
ENST00000636152.1:n.53-198_53-194delinsCTATT
ENST00000675732.1:c.1316-198_1316-194delinsCTATT	ENSP00000502598.1:n.1316-198_1316-194delinsCTATT
ENST00000373344.9:c.6218-198_6218-194delinsCTATT	ENSP00000362441.4:n.6218-198_6218-194delinsCTATT
ENST00000395603.7:c.6104-198_6104-194delinsCTATT	ENSP00000378967.3:n.6104-198_6104-194delinsCTATT
ENST00000480283.5:c.*5846-198_*5846-194delinsCTATT	ENSP00000480196.1:n.*5846-198_*5846-194delinsCTATT
ENST00000623316.1:c.702-198_702-194delinsCTATT
ENST00000623706.3:n.3288-198_3288-194delinsCTATT
NM_000489.4:c.6218-198_6218-194delinsCTATT	NP_000480.3:n.6218-198_6218-194delinsCTATT
NM_138270.3:c.6104-198_6104-194delinsCTATT	NP_612114.2:n.6104-198_6104-194delinsCTATT
XM_005262153.3:c.6215-198_6215-194delinsCTATT	XP_005262210.2:n.6215-198_6215-194delinsCTATT
XM_005262154.3:c.6131-198_6131-194delinsCTATT	XP_005262211.2:n.6131-198_6131-194delinsCTATT
XM_005262155.3:c.6101-198_6101-194delinsCTATT	XP_005262212.2:n.6101-198_6101-194delinsCTATT
XM_005262156.3:c.6053-198_6053-194delinsCTATT	XP_005262213.2:n.6053-198_6053-194delinsCTATT
XM_005262157.3:c.6014-198_6014-194delinsCTATT	XP_005262214.2:n.6014-198_6014-194delinsCTATT
XM_006724666.2:c.6101-198_6101-194delinsCTATT	XP_006724729.1:n.6101-198_6101-194delinsCTATT
XM_006724667.2:c.5939-198_5939-194delinsCTATT	XP_006724730.1:n.5939-198_5939-194delinsCTATT
XR_938400.1:n.6560-198_6560-194delinsCTATT
NM_000489.5:c.6218-198_6218-194delinsCTATT	NP_000480.3:n.6218-198_6218-194delinsCTATT
XM_005262153.5:c.6215-198_6215-194delinsCTATT	XP_005262210.2:n.6215-198_6215-194delinsCTATT
XM_005262154.5:c.6131-198_6131-194delinsCTATT	XP_005262211.2:n.6131-198_6131-194delinsCTATT
XM_005262155.4:c.6101-198_6101-194delinsCTATT	XP_005262212.2:n.6101-198_6101-194delinsCTATT
XM_005262156.4:c.6053-198_6053-194delinsCTATT	XP_005262213.2:n.6053-198_6053-194delinsCTATT
XM_005262157.5:c.6014-198_6014-194delinsCTATT	XP_005262214.2:n.6014-198_6014-194delinsCTATT
XM_006724666.4:c.6101-198_6101-194delinsCTATT	XP_006724729.1:n.6101-198_6101-194delinsCTATT
XM_006724667.3:c.5939-198_5939-194delinsCTATT	XP_006724730.1:n.5939-198_5939-194delinsCTATT
XM_017029601.2:c.6128-198_6128-194delinsCTATT	XP_016885090.1:n.6128-198_6128-194delinsCTATT
XM_017029602.1:c.6098-198_6098-194delinsCTATT	XP_016885091.1:n.6098-198_6098-194delinsCTATT
XM_017029603.1:c.6050-198_6050-194delinsCTATT	XP_016885092.1:n.6050-198_6050-194delinsCTATT
XM_017029604.2:c.6017-198_6017-194delinsCTATT	XP_016885093.1:n.6017-198_6017-194delinsCTATT
XM_017029605.1:c.6014-198_6014-194delinsCTATT	XP_016885094.1:n.6014-198_6014-194delinsCTATT
XM_017029606.2:c.5987-198_5987-194delinsCTATT	XP_016885095.1:n.5987-198_5987-194delinsCTATT
XM_017029607.2:c.5984-198_5984-194delinsCTATT	XP_016885096.1:n.5984-198_5984-194delinsCTATT
XM_017029608.2:c.5936-198_5936-194delinsCTATT	XP_016885097.1:n.5936-198_5936-194delinsCTATT
XM_017029609.1:c.5900-198_5900-194delinsCTATT	XP_016885098.1:n.5900-198_5900-194delinsCTATT
XM_017029610.1:c.5897-198_5897-194delinsCTATT	XP_016885099.1:n.5897-198_5897-194delinsCTATT
XM_017029611.1:c.5852-198_5852-194delinsCTATT	XP_016885100.1:n.5852-198_5852-194delinsCTATT
XR_001755700.2:n.6517-198_6517-194delinsCTATT
NM_138270.4:c.6104-198_6104-194delinsCTATT	NP_612114.2:n.6104-198_6104-194delinsCTATT
NM_000489.6:c.6218-198_6218-194delinsCTATT MANE Select	NP_000480.3:n.6218-198_6218-194delinsCTATT
NM_138270.5:c.6104-198_6104-194delinsCTATT	NP_612114.2:n.6104-198_6104-194delinsCTATT