Canonical Allele Identifier: CA517374767

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829756C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574291C>T , CM000685.2:g.77574291C>T	GRCh38
NC_000023.10:g.76829756C>T , CM000685.1:g.76829756C>T	GRCh37
NC_000023.9:g.76716412C>T	NCBI36
NG_008838.2:g.216931G>A
NG_008838.3:g.216979G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6285G>A MANE Select	ENSP00000362441.4:p.Arg2095=
ENST00000675732.1:c.1383G>A	ENSP00000502598.1:p.Arg461=
ENST00000373344.9:c.6285G>A	ENSP00000362441.4:p.Arg2095=
ENST00000395603.7:c.6171G>A	ENSP00000378967.3:p.Arg2057=
ENST00000480283.5:c.*5913G>A	ENSP00000480196.1:n.*5913G>A
ENST00000623316.1:c.769G>A
ENST00000623706.3:n.3355G>A
NM_000489.4:c.6285G>A	NP_000480.3:p.Arg2095=
NM_138270.3:c.6171G>A	NP_612114.2:p.Arg2057=
XM_005262153.3:c.6282G>A	XP_005262210.2:p.Arg2094=
XM_005262154.3:c.6198G>A	XP_005262211.2:p.Arg2066=
XM_005262155.3:c.6168G>A	XP_005262212.2:p.Arg2056=
XM_005262156.3:c.6120G>A	XP_005262213.2:p.Arg2040=
XM_005262157.3:c.6081G>A	XP_005262214.2:p.Arg2027=
XM_006724666.2:c.6168G>A	XP_006724729.1:p.Arg2056=
XM_006724667.2:c.6006G>A	XP_006724730.1:p.Arg2002=
XR_938400.1:n.6627G>A
NM_000489.5:c.6285G>A	NP_000480.3:p.Arg2095=
XM_005262153.5:c.6282G>A	XP_005262210.2:p.Arg2094=
XM_005262154.5:c.6198G>A	XP_005262211.2:p.Arg2066=
XM_005262155.4:c.6168G>A	XP_005262212.2:p.Arg2056=
XM_005262156.4:c.6120G>A	XP_005262213.2:p.Arg2040=
XM_005262157.5:c.6081G>A	XP_005262214.2:p.Arg2027=
XM_006724666.4:c.6168G>A	XP_006724729.1:p.Arg2056=
XM_006724667.3:c.6006G>A	XP_006724730.1:p.Arg2002=
XM_017029601.2:c.6195G>A	XP_016885090.1:p.Arg2065=
XM_017029602.1:c.6165G>A	XP_016885091.1:p.Arg2055=
XM_017029603.1:c.6117G>A	XP_016885092.1:p.Arg2039=
XM_017029604.2:c.6084G>A	XP_016885093.1:p.Arg2028=
XM_017029605.1:c.6081G>A	XP_016885094.1:p.Arg2027=
XM_017029606.2:c.6054G>A	XP_016885095.1:p.Arg2018=
XM_017029607.2:c.6051G>A	XP_016885096.1:p.Arg2017=
XM_017029608.2:c.6003G>A	XP_016885097.1:p.Arg2001=
XM_017029609.1:c.5967G>A	XP_016885098.1:p.Arg1989=
XM_017029610.1:c.5964G>A	XP_016885099.1:p.Arg1988=
XM_017029611.1:c.5919G>A	XP_016885100.1:p.Arg1973=
XR_001755700.2:n.6584G>A
NM_138270.4:c.6171G>A	NP_612114.2:p.Arg2057=
NM_000489.6:c.6285G>A MANE Select	NP_000480.3:p.Arg2095=
NM_138270.5:c.6171G>A	NP_612114.2:p.Arg2057=