Canonical Allele Identifier: CA517471128

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907616T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652126T>C , CM000685.2:g.77652126T>C	GRCh38
NC_000023.10:g.76907616T>C , CM000685.1:g.76907616T>C	GRCh37
NC_000023.9:g.76794272T>C	NCBI36
NG_008838.2:g.139096A>G
NG_008838.3:g.139144A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4545A>G MANE Select	ENSP00000362441.4:p.Glu1515=
ENST00000373344.9:c.4545A>G	ENSP00000362441.4:p.Glu1515=
ENST00000395603.7:c.4431A>G	ENSP00000378967.3:p.Glu1477=
ENST00000460639.2:n.25A>G
ENST00000480283.5:c.*4173A>G	ENSP00000480196.1:n.*4173A>G
ENST00000623242.3:c.151A>G
NM_000489.4:c.4545A>G	NP_000480.3:p.Glu1515=
NM_138270.3:c.4431A>G	NP_612114.2:p.Glu1477=
XM_005262153.3:c.4542A>G	XP_005262210.2:p.Glu1514=
XM_005262154.3:c.4458A>G	XP_005262211.2:p.Glu1486=
XM_005262155.3:c.4428A>G	XP_005262212.2:p.Glu1476=
XM_005262156.3:c.4380A>G	XP_005262213.2:p.Glu1460=
XM_005262157.3:c.4341A>G	XP_005262214.2:p.Glu1447=
XM_006724666.2:c.4428A>G	XP_006724729.1:p.Glu1476=
XM_006724667.2:c.4266A>G	XP_006724730.1:p.Glu1422=
XM_006724668.2:c.4545A>G	XP_006724731.1:p.Glu1515=
XR_938400.1:n.4813A>G
NM_000489.5:c.4545A>G	NP_000480.3:p.Glu1515=
XM_005262153.5:c.4542A>G	XP_005262210.2:p.Glu1514=
XM_005262154.5:c.4458A>G	XP_005262211.2:p.Glu1486=
XM_005262155.4:c.4428A>G	XP_005262212.2:p.Glu1476=
XM_005262156.4:c.4380A>G	XP_005262213.2:p.Glu1460=
XM_005262157.5:c.4341A>G	XP_005262214.2:p.Glu1447=
XM_006724666.4:c.4428A>G	XP_006724729.1:p.Glu1476=
XM_006724667.3:c.4266A>G	XP_006724730.1:p.Glu1422=
XM_006724668.3:c.4545A>G	XP_006724731.1:p.Glu1515=
XM_017029601.2:c.4455A>G	XP_016885090.1:p.Glu1485=
XM_017029602.1:c.4425A>G	XP_016885091.1:p.Glu1475=
XM_017029603.1:c.4377A>G	XP_016885092.1:p.Glu1459=
XM_017029604.2:c.4344A>G	XP_016885093.1:p.Glu1448=
XM_017029605.1:c.4341A>G	XP_016885094.1:p.Glu1447=
XM_017029606.2:c.4314A>G	XP_016885095.1:p.Glu1438=
XM_017029607.2:c.4311A>G	XP_016885096.1:p.Glu1437=
XM_017029608.2:c.4263A>G	XP_016885097.1:p.Glu1421=
XM_017029609.1:c.4227A>G	XP_016885098.1:p.Glu1409=
XM_017029610.1:c.4224A>G	XP_016885099.1:p.Glu1408=
XM_017029611.1:c.4179A>G	XP_016885100.1:p.Glu1393=
XR_001755700.2:n.4770A>G
NM_138270.4:c.4431A>G	NP_612114.2:p.Glu1477=
NM_000489.6:c.4545A>G MANE Select	NP_000480.3:p.Glu1515=
NM_138270.5:c.4431A>G	NP_612114.2:p.Glu1477=