Canonical Allele Identifier: CA413708874

Gene: ATRX

Linked Data

• dbSNP Id: rs2069290885
• MyVariant Identifiers: chrX:g.76907813C>T (hg19) ; chrX:g.77652323C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652323C>T , CM000685.2:g.77652323C>T	GRCh38
NC_000023.10:g.76907813C>T , CM000685.1:g.76907813C>T	GRCh37
NC_000023.9:g.76794469C>T	NCBI36
NG_008838.2:g.138899G>A
NG_008838.3:g.138947G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4348G>A MANE Select	ENSP00000362441.4:p.Glu1450Lys
ENST00000373344.9:c.4348G>A	ENSP00000362441.4:p.Glu1450Lys
ENST00000395603.7:c.4234G>A	ENSP00000378967.3:p.Glu1412Lys
ENST00000480283.5:c.*3976G>A	ENSP00000480196.1:n.*3976G>A
NM_000489.4:c.4348G>A	NP_000480.3:p.Glu1450Lys
NM_138270.3:c.4234G>A	NP_612114.2:p.Glu1412Lys
XM_005262153.3:c.4345G>A	XP_005262210.2:p.Glu1449Lys
XM_005262154.3:c.4261G>A	XP_005262211.2:p.Glu1421Lys
XM_005262155.3:c.4231G>A	XP_005262212.2:p.Glu1411Lys
XM_005262156.3:c.4183G>A	XP_005262213.2:p.Glu1395Lys
XM_005262157.3:c.4144G>A	XP_005262214.2:p.Glu1382Lys
XM_006724666.2:c.4231G>A	XP_006724729.1:p.Glu1411Lys
XM_006724667.2:c.4069G>A	XP_006724730.1:p.Glu1357Lys
XM_006724668.2:c.4348G>A	XP_006724731.1:p.Glu1450Lys
XR_938400.1:n.4616G>A
NM_000489.5:c.4348G>A	NP_000480.3:p.Glu1450Lys
XM_005262153.5:c.4345G>A	XP_005262210.2:p.Glu1449Lys
XM_005262154.5:c.4261G>A	XP_005262211.2:p.Glu1421Lys
XM_005262155.4:c.4231G>A	XP_005262212.2:p.Glu1411Lys
XM_005262156.4:c.4183G>A	XP_005262213.2:p.Glu1395Lys
XM_005262157.5:c.4144G>A	XP_005262214.2:p.Glu1382Lys
XM_006724666.4:c.4231G>A	XP_006724729.1:p.Glu1411Lys
XM_006724667.3:c.4069G>A	XP_006724730.1:p.Glu1357Lys
XM_006724668.3:c.4348G>A	XP_006724731.1:p.Glu1450Lys
XM_017029601.2:c.4258G>A	XP_016885090.1:p.Glu1420Lys
XM_017029602.1:c.4228G>A	XP_016885091.1:p.Glu1410Lys
XM_017029603.1:c.4180G>A	XP_016885092.1:p.Glu1394Lys
XM_017029604.2:c.4147G>A	XP_016885093.1:p.Glu1383Lys
XM_017029605.1:c.4144G>A	XP_016885094.1:p.Glu1382Lys
XM_017029606.2:c.4117G>A	XP_016885095.1:p.Glu1373Lys
XM_017029607.2:c.4114G>A	XP_016885096.1:p.Glu1372Lys
XM_017029608.2:c.4066G>A	XP_016885097.1:p.Glu1356Lys
XM_017029609.1:c.4030G>A	XP_016885098.1:p.Glu1344Lys
XM_017029610.1:c.4027G>A	XP_016885099.1:p.Glu1343Lys
XM_017029611.1:c.3982G>A	XP_016885100.1:p.Glu1328Lys
XR_001755700.2:n.4573G>A
NM_138270.4:c.4234G>A	NP_612114.2:p.Glu1412Lys
NM_000489.6:c.4348G>A MANE Select	NP_000480.3:p.Glu1450Lys
NM_138270.5:c.4234G>A	NP_612114.2:p.Glu1412Lys