Canonical Allele Identifier: CA2738724188

Gene: ATRX

Linked Data

• dbSNP Id: rs2147647674

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508446del , CM000685.2:g.77508446del	GRCh38
NC_000023.10:g.76763924del , CM000685.1:g.76763924del	GRCh37
NC_000023.9:g.76650580del	NCBI36
NG_008838.2:g.282777del
NG_008838.3:g.282825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7385del MANE Select	ENSP00000362441.4:p.Pro2462GlnfsTer18
ENST00000675732.1:c.2483del	ENSP00000502598.1:p.Pro828GlnfsTer18
ENST00000373344.9:c.7385del	ENSP00000362441.4:p.Pro2462GlnfsTer18
ENST00000395603.7:c.7271del	ENSP00000378967.3:p.Pro2424GlnfsTer18
ENST00000480283.5:c.*7013del	ENSP00000480196.1:n.*7013del
ENST00000623706.3:n.5705del
NM_000489.4:c.7385del	NP_000480.3:p.Pro2462GlnfsTer18
NM_138270.3:c.7271del	NP_612114.2:p.Pro2424GlnfsTer18
XM_005262153.3:c.7382del	XP_005262210.2:p.Pro2461GlnfsTer18
XM_005262154.3:c.7298del	XP_005262211.2:p.Pro2433GlnfsTer18
XM_005262155.3:c.7268del	XP_005262212.2:p.Pro2423GlnfsTer18
XM_005262156.3:c.7220del	XP_005262213.2:p.Pro2407GlnfsTer18
XM_005262157.3:c.7181del	XP_005262214.2:p.Pro2394GlnfsTer18
XM_006724666.2:c.7268del	XP_006724729.1:p.Pro2423GlnfsTer18
XM_006724667.2:c.7106del	XP_006724730.1:p.Pro2369GlnfsTer18
XR_938400.1:n.8977del
NM_000489.5:c.7385del	NP_000480.3:p.Pro2462GlnfsTer18
XM_005262153.5:c.7382del	XP_005262210.2:p.Pro2461GlnfsTer18
XM_005262154.5:c.7298del	XP_005262211.2:p.Pro2433GlnfsTer18
XM_005262155.4:c.7268del	XP_005262212.2:p.Pro2423GlnfsTer18
XM_005262156.4:c.7220del	XP_005262213.2:p.Pro2407GlnfsTer18
XM_005262157.5:c.7181del	XP_005262214.2:p.Pro2394GlnfsTer18
XM_006724666.4:c.7268del	XP_006724729.1:p.Pro2423GlnfsTer18
XM_006724667.3:c.7106del	XP_006724730.1:p.Pro2369GlnfsTer18
XM_017029601.2:c.7295del	XP_016885090.1:p.Pro2432GlnfsTer18
XM_017029602.1:c.7265del	XP_016885091.1:p.Pro2422GlnfsTer18
XM_017029603.1:c.7217del	XP_016885092.1:p.Pro2406GlnfsTer18
XM_017029604.2:c.7184del	XP_016885093.1:p.Pro2395GlnfsTer18
XM_017029605.1:c.7181del	XP_016885094.1:p.Pro2394GlnfsTer18
XM_017029606.2:c.7154del	XP_016885095.1:p.Pro2385GlnfsTer18
XM_017029607.2:c.7151del	XP_016885096.1:p.Pro2384GlnfsTer18
XM_017029608.2:c.7103del	XP_016885097.1:p.Pro2368GlnfsTer18
XM_017029609.1:c.7067del	XP_016885098.1:p.Pro2356GlnfsTer18
XM_017029610.1:c.7064del	XP_016885099.1:p.Pro2355GlnfsTer18
XM_017029611.1:c.7019del	XP_016885100.1:p.Pro2340GlnfsTer18
XR_001755700.2:n.7684del
NM_138270.4:c.7271del	NP_612114.2:p.Pro2424GlnfsTer18
NM_000489.6:c.7385del MANE Select	NP_000480.3:p.Pro2462GlnfsTer18
NM_138270.5:c.7271del	NP_612114.2:p.Pro2424GlnfsTer18