Canonical Allele Identifier: CA517471480

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907739T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652249T>A , CM000685.2:g.77652249T>A	GRCh38
NC_000023.10:g.76907739T>A , CM000685.1:g.76907739T>A	GRCh37
NC_000023.9:g.76794395T>A	NCBI36
NG_008838.2:g.138973A>T
NG_008838.3:g.139021A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4422A>T MANE Select	ENSP00000362441.4:p.Gly1474=
ENST00000373344.9:c.4422A>T	ENSP00000362441.4:p.Gly1474=
ENST00000395603.7:c.4308A>T	ENSP00000378967.3:p.Gly1436=
ENST00000480283.5:c.*4050A>T	ENSP00000480196.1:n.*4050A>T
ENST00000623242.3:c.28A>T
NM_000489.4:c.4422A>T	NP_000480.3:p.Gly1474=
NM_138270.3:c.4308A>T	NP_612114.2:p.Gly1436=
XM_005262153.3:c.4419A>T	XP_005262210.2:p.Gly1473=
XM_005262154.3:c.4335A>T	XP_005262211.2:p.Gly1445=
XM_005262155.3:c.4305A>T	XP_005262212.2:p.Gly1435=
XM_005262156.3:c.4257A>T	XP_005262213.2:p.Gly1419=
XM_005262157.3:c.4218A>T	XP_005262214.2:p.Gly1406=
XM_006724666.2:c.4305A>T	XP_006724729.1:p.Gly1435=
XM_006724667.2:c.4143A>T	XP_006724730.1:p.Gly1381=
XM_006724668.2:c.4422A>T	XP_006724731.1:p.Gly1474=
XR_938400.1:n.4690A>T
NM_000489.5:c.4422A>T	NP_000480.3:p.Gly1474=
XM_005262153.5:c.4419A>T	XP_005262210.2:p.Gly1473=
XM_005262154.5:c.4335A>T	XP_005262211.2:p.Gly1445=
XM_005262155.4:c.4305A>T	XP_005262212.2:p.Gly1435=
XM_005262156.4:c.4257A>T	XP_005262213.2:p.Gly1419=
XM_005262157.5:c.4218A>T	XP_005262214.2:p.Gly1406=
XM_006724666.4:c.4305A>T	XP_006724729.1:p.Gly1435=
XM_006724667.3:c.4143A>T	XP_006724730.1:p.Gly1381=
XM_006724668.3:c.4422A>T	XP_006724731.1:p.Gly1474=
XM_017029601.2:c.4332A>T	XP_016885090.1:p.Gly1444=
XM_017029602.1:c.4302A>T	XP_016885091.1:p.Gly1434=
XM_017029603.1:c.4254A>T	XP_016885092.1:p.Gly1418=
XM_017029604.2:c.4221A>T	XP_016885093.1:p.Gly1407=
XM_017029605.1:c.4218A>T	XP_016885094.1:p.Gly1406=
XM_017029606.2:c.4191A>T	XP_016885095.1:p.Gly1397=
XM_017029607.2:c.4188A>T	XP_016885096.1:p.Gly1396=
XM_017029608.2:c.4140A>T	XP_016885097.1:p.Gly1380=
XM_017029609.1:c.4104A>T	XP_016885098.1:p.Gly1368=
XM_017029610.1:c.4101A>T	XP_016885099.1:p.Gly1367=
XM_017029611.1:c.4056A>T	XP_016885100.1:p.Gly1352=
XR_001755700.2:n.4647A>T
NM_138270.4:c.4308A>T	NP_612114.2:p.Gly1436=
NM_000489.6:c.4422A>T MANE Select	NP_000480.3:p.Gly1474=
NM_138270.5:c.4308A>T	NP_612114.2:p.Gly1436=