Canonical Allele Identifier: CA2738724322

Gene: ATRX

Linked Data

• dbSNP Id: rs2147651308

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508564_77508572del , CM000685.2:g.77508564_77508572del	GRCh38
NC_000023.10:g.76764042_76764050del , CM000685.1:g.76764042_76764050del	GRCh37
NC_000023.9:g.76650698_76650706del	NCBI36
NG_008838.2:g.282655_282663del
NG_008838.3:g.282703_282711del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7263_7271del MANE Select	ENSP00000362441.4:p.Gln2422_Gln2424del
ENST00000675732.1:c.2361_2369del	ENSP00000502598.1:p.Gln788_Gln790del
ENST00000373344.9:c.7263_7271del	ENSP00000362441.4:p.Gln2422_Gln2424del
ENST00000395603.7:c.7149_7157del	ENSP00000378967.3:p.Gln2384_Gln2386del
ENST00000480283.5:c.*6891_*6899del	ENSP00000480196.1:n.*6891_*6899del
ENST00000623706.3:n.5583_5591del
ENST00000624766.1:n.494_502del
NM_000489.4:c.7263_7271del	NP_000480.3:p.Gln2422_Gln2424del
NM_138270.3:c.7149_7157del	NP_612114.2:p.Gln2384_Gln2386del
XM_005262153.3:c.7260_7268del	XP_005262210.2:p.Gln2421_Gln2423del
XM_005262154.3:c.7176_7184del	XP_005262211.2:p.Gln2393_Gln2395del
XM_005262155.3:c.7146_7154del	XP_005262212.2:p.Gln2383_Gln2385del
XM_005262156.3:c.7098_7106del	XP_005262213.2:p.Gln2367_Gln2369del
XM_005262157.3:c.7059_7067del	XP_005262214.2:p.Gln2354_Gln2356del
XM_006724666.2:c.7146_7154del	XP_006724729.1:p.Gln2383_Gln2385del
XM_006724667.2:c.6984_6992del	XP_006724730.1:p.Gln2329_Gln2331del
XR_938400.1:n.8855_8863del
NM_000489.5:c.7263_7271del	NP_000480.3:p.Gln2422_Gln2424del
XM_005262153.5:c.7260_7268del	XP_005262210.2:p.Gln2421_Gln2423del
XM_005262154.5:c.7176_7184del	XP_005262211.2:p.Gln2393_Gln2395del
XM_005262155.4:c.7146_7154del	XP_005262212.2:p.Gln2383_Gln2385del
XM_005262156.4:c.7098_7106del	XP_005262213.2:p.Gln2367_Gln2369del
XM_005262157.5:c.7059_7067del	XP_005262214.2:p.Gln2354_Gln2356del
XM_006724666.4:c.7146_7154del	XP_006724729.1:p.Gln2383_Gln2385del
XM_006724667.3:c.6984_6992del	XP_006724730.1:p.Gln2329_Gln2331del
XM_017029601.2:c.7173_7181del	XP_016885090.1:p.Gln2392_Gln2394del
XM_017029602.1:c.7143_7151del	XP_016885091.1:p.Gln2382_Gln2384del
XM_017029603.1:c.7095_7103del	XP_016885092.1:p.Gln2366_Gln2368del
XM_017029604.2:c.7062_7070del	XP_016885093.1:p.Gln2355_Gln2357del
XM_017029605.1:c.7059_7067del	XP_016885094.1:p.Gln2354_Gln2356del
XM_017029606.2:c.7032_7040del	XP_016885095.1:p.Gln2345_Gln2347del
XM_017029607.2:c.7029_7037del	XP_016885096.1:p.Gln2344_Gln2346del
XM_017029608.2:c.6981_6989del	XP_016885097.1:p.Gln2328_Gln2330del
XM_017029609.1:c.6945_6953del	XP_016885098.1:p.Gln2316_Gln2318del
XM_017029610.1:c.6942_6950del	XP_016885099.1:p.Gln2315_Gln2317del
XM_017029611.1:c.6897_6905del	XP_016885100.1:p.Gln2300_Gln2302del
XR_001755700.2:n.7562_7570del
NM_138270.4:c.7149_7157del	NP_612114.2:p.Gln2384_Gln2386del
NM_000489.6:c.7263_7271del MANE Select	NP_000480.3:p.Gln2422_Gln2424del
NM_138270.5:c.7149_7157del	NP_612114.2:p.Gln2384_Gln2386del