Canonical Allele Identifier: CA2438929046

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508451T= , CM000685.2:g.77508451T=	GRCh38
NC_000023.10:g.76763929T= , CM000685.1:g.76763929T=	GRCh37
NC_000023.9:g.76650585T=	NCBI36
NG_008838.2:g.282771A=
NG_008838.3:g.282819A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7379A= MANE Select	ENSP00000362441.4:p.Tyr2460=
ENST00000675732.1:c.2477A=	ENSP00000502598.1:p.Tyr826=
ENST00000373344.9:c.7379A=	ENSP00000362441.4:p.Tyr2460=
ENST00000395603.7:c.7265A=	ENSP00000378967.3:p.Tyr2422=
ENST00000480283.5:c.*7007A=	ENSP00000480196.1:n.*7007A=
ENST00000623706.3:n.5699A=
NM_000489.4:c.7379A=	NP_000480.3:p.Tyr2460=
NM_138270.3:c.7265A=	NP_612114.2:p.Tyr2422=
XM_005262153.3:c.7376A=	XP_005262210.2:p.Tyr2459=
XM_005262154.3:c.7292A=	XP_005262211.2:p.Tyr2431=
XM_005262155.3:c.7262A=	XP_005262212.2:p.Tyr2421=
XM_005262156.3:c.7214A=	XP_005262213.2:p.Tyr2405=
XM_005262157.3:c.7175A=	XP_005262214.2:p.Tyr2392=
XM_006724666.2:c.7262A=	XP_006724729.1:p.Tyr2421=
XM_006724667.2:c.7100A=	XP_006724730.1:p.Tyr2367=
XR_938400.1:n.8971A=
NM_000489.5:c.7379A=	NP_000480.3:p.Tyr2460=
XM_005262153.5:c.7376A=	XP_005262210.2:p.Tyr2459=
XM_005262154.5:c.7292A=	XP_005262211.2:p.Tyr2431=
XM_005262155.4:c.7262A=	XP_005262212.2:p.Tyr2421=
XM_005262156.4:c.7214A=	XP_005262213.2:p.Tyr2405=
XM_005262157.5:c.7175A=	XP_005262214.2:p.Tyr2392=
XM_006724666.4:c.7262A=	XP_006724729.1:p.Tyr2421=
XM_006724667.3:c.7100A=	XP_006724730.1:p.Tyr2367=
XM_017029601.2:c.7289A=	XP_016885090.1:p.Tyr2430=
XM_017029602.1:c.7259A=	XP_016885091.1:p.Tyr2420=
XM_017029603.1:c.7211A=	XP_016885092.1:p.Tyr2404=
XM_017029604.2:c.7178A=	XP_016885093.1:p.Tyr2393=
XM_017029605.1:c.7175A=	XP_016885094.1:p.Tyr2392=
XM_017029606.2:c.7148A=	XP_016885095.1:p.Tyr2383=
XM_017029607.2:c.7145A=	XP_016885096.1:p.Tyr2382=
XM_017029608.2:c.7097A=	XP_016885097.1:p.Tyr2366=
XM_017029609.1:c.7061A=	XP_016885098.1:p.Tyr2354=
XM_017029610.1:c.7058A=	XP_016885099.1:p.Tyr2353=
XM_017029611.1:c.7013A=	XP_016885100.1:p.Tyr2338=
XR_001755700.2:n.7678A=
NM_138270.4:c.7265A=	NP_612114.2:p.Tyr2422=
NM_000489.6:c.7379A= MANE Select	NP_000480.3:p.Tyr2460=
NM_138270.5:c.7265A=	NP_612114.2:p.Tyr2422=