Canonical Allele Identifier: CA413708763

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907796C>A (hg19) ; chrX:g.77652306C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652306C>A , CM000685.2:g.77652306C>A	GRCh38
NC_000023.10:g.76907796C>A , CM000685.1:g.76907796C>A	GRCh37
NC_000023.9:g.76794452C>A	NCBI36
NG_008838.2:g.138916G>T
NG_008838.3:g.138964G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4365G>T MANE Select	ENSP00000362441.4:p.Glu1455Asp
ENST00000373344.9:c.4365G>T	ENSP00000362441.4:p.Glu1455Asp
ENST00000395603.7:c.4251G>T	ENSP00000378967.3:p.Glu1417Asp
ENST00000480283.5:c.*3993G>T	ENSP00000480196.1:n.*3993G>T
NM_000489.4:c.4365G>T	NP_000480.3:p.Glu1455Asp
NM_138270.3:c.4251G>T	NP_612114.2:p.Glu1417Asp
XM_005262153.3:c.4362G>T	XP_005262210.2:p.Glu1454Asp
XM_005262154.3:c.4278G>T	XP_005262211.2:p.Glu1426Asp
XM_005262155.3:c.4248G>T	XP_005262212.2:p.Glu1416Asp
XM_005262156.3:c.4200G>T	XP_005262213.2:p.Glu1400Asp
XM_005262157.3:c.4161G>T	XP_005262214.2:p.Glu1387Asp
XM_006724666.2:c.4248G>T	XP_006724729.1:p.Glu1416Asp
XM_006724667.2:c.4086G>T	XP_006724730.1:p.Glu1362Asp
XM_006724668.2:c.4365G>T	XP_006724731.1:p.Glu1455Asp
XR_938400.1:n.4633G>T
NM_000489.5:c.4365G>T	NP_000480.3:p.Glu1455Asp
XM_005262153.5:c.4362G>T	XP_005262210.2:p.Glu1454Asp
XM_005262154.5:c.4278G>T	XP_005262211.2:p.Glu1426Asp
XM_005262155.4:c.4248G>T	XP_005262212.2:p.Glu1416Asp
XM_005262156.4:c.4200G>T	XP_005262213.2:p.Glu1400Asp
XM_005262157.5:c.4161G>T	XP_005262214.2:p.Glu1387Asp
XM_006724666.4:c.4248G>T	XP_006724729.1:p.Glu1416Asp
XM_006724667.3:c.4086G>T	XP_006724730.1:p.Glu1362Asp
XM_006724668.3:c.4365G>T	XP_006724731.1:p.Glu1455Asp
XM_017029601.2:c.4275G>T	XP_016885090.1:p.Glu1425Asp
XM_017029602.1:c.4245G>T	XP_016885091.1:p.Glu1415Asp
XM_017029603.1:c.4197G>T	XP_016885092.1:p.Glu1399Asp
XM_017029604.2:c.4164G>T	XP_016885093.1:p.Glu1388Asp
XM_017029605.1:c.4161G>T	XP_016885094.1:p.Glu1387Asp
XM_017029606.2:c.4134G>T	XP_016885095.1:p.Glu1378Asp
XM_017029607.2:c.4131G>T	XP_016885096.1:p.Glu1377Asp
XM_017029608.2:c.4083G>T	XP_016885097.1:p.Glu1361Asp
XM_017029609.1:c.4047G>T	XP_016885098.1:p.Glu1349Asp
XM_017029610.1:c.4044G>T	XP_016885099.1:p.Glu1348Asp
XM_017029611.1:c.3999G>T	XP_016885100.1:p.Glu1333Asp
XR_001755700.2:n.4590G>T
NM_138270.4:c.4251G>T	NP_612114.2:p.Glu1417Asp
NM_000489.6:c.4365G>T MANE Select	NP_000480.3:p.Glu1455Asp
NM_138270.5:c.4251G>T	NP_612114.2:p.Glu1417Asp