Canonical Allele Identifier: CA2738724161

Gene: ATRX

Linked Data

• dbSNP Id: rs2147646808

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508422del , CM000685.2:g.77508422del	GRCh38
NC_000023.10:g.76763900del , CM000685.1:g.76763900del	GRCh37
NC_000023.9:g.76650556del	NCBI36
NG_008838.2:g.282801del
NG_008838.3:g.282849del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7409del MANE Select	ENSP00000362441.4:p.Pro2470HisfsTer10
ENST00000675732.1:c.2507del	ENSP00000502598.1:p.Pro836HisfsTer10
ENST00000373344.9:c.7409del	ENSP00000362441.4:p.Pro2470HisfsTer10
ENST00000395603.7:c.7295del	ENSP00000378967.3:p.Pro2432HisfsTer10
ENST00000480283.5:c.*7037del	ENSP00000480196.1:n.*7037del
ENST00000623706.3:n.5729del
NM_000489.4:c.7409del	NP_000480.3:p.Pro2470HisfsTer10
NM_138270.3:c.7295del	NP_612114.2:p.Pro2432HisfsTer10
XM_005262153.3:c.7406del	XP_005262210.2:p.Pro2469HisfsTer10
XM_005262154.3:c.7322del	XP_005262211.2:p.Pro2441HisfsTer10
XM_005262155.3:c.7292del	XP_005262212.2:p.Pro2431HisfsTer10
XM_005262156.3:c.7244del	XP_005262213.2:p.Pro2415HisfsTer10
XM_005262157.3:c.7205del	XP_005262214.2:p.Pro2402HisfsTer10
XM_006724666.2:c.7292del	XP_006724729.1:p.Pro2431HisfsTer10
XM_006724667.2:c.7130del	XP_006724730.1:p.Pro2377HisfsTer10
XR_938400.1:n.9001del
NM_000489.5:c.7409del	NP_000480.3:p.Pro2470HisfsTer10
XM_005262153.5:c.7406del	XP_005262210.2:p.Pro2469HisfsTer10
XM_005262154.5:c.7322del	XP_005262211.2:p.Pro2441HisfsTer10
XM_005262155.4:c.7292del	XP_005262212.2:p.Pro2431HisfsTer10
XM_005262156.4:c.7244del	XP_005262213.2:p.Pro2415HisfsTer10
XM_005262157.5:c.7205del	XP_005262214.2:p.Pro2402HisfsTer10
XM_006724666.4:c.7292del	XP_006724729.1:p.Pro2431HisfsTer10
XM_006724667.3:c.7130del	XP_006724730.1:p.Pro2377HisfsTer10
XM_017029601.2:c.7319del	XP_016885090.1:p.Pro2440HisfsTer10
XM_017029602.1:c.7289del	XP_016885091.1:p.Pro2430HisfsTer10
XM_017029603.1:c.7241del	XP_016885092.1:p.Pro2414HisfsTer10
XM_017029604.2:c.7208del	XP_016885093.1:p.Pro2403HisfsTer10
XM_017029605.1:c.7205del	XP_016885094.1:p.Pro2402HisfsTer10
XM_017029606.2:c.7178del	XP_016885095.1:p.Pro2393HisfsTer10
XM_017029607.2:c.7175del	XP_016885096.1:p.Pro2392HisfsTer10
XM_017029608.2:c.7127del	XP_016885097.1:p.Pro2376HisfsTer10
XM_017029609.1:c.7091del	XP_016885098.1:p.Pro2364HisfsTer10
XM_017029610.1:c.7088del	XP_016885099.1:p.Pro2363HisfsTer10
XM_017029611.1:c.7043del	XP_016885100.1:p.Pro2348HisfsTer10
XR_001755700.2:n.7708del
NM_138270.4:c.7295del	NP_612114.2:p.Pro2432HisfsTer10
NM_000489.6:c.7409del MANE Select	NP_000480.3:p.Pro2470HisfsTer10
NM_138270.5:c.7295del	NP_612114.2:p.Pro2432HisfsTer10