Canonical Allele Identifier: CA517374740

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829716T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574251T>G , CM000685.2:g.77574251T>G	GRCh38
NC_000023.10:g.76829716T>G , CM000685.1:g.76829716T>G	GRCh37
NC_000023.9:g.76716372T>G	NCBI36
NG_008838.2:g.216971A>C
NG_008838.3:g.217019A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6325A>C MANE Select	ENSP00000362441.4:p.Arg2109=
ENST00000675732.1:c.1423A>C	ENSP00000502598.1:p.Arg475=
ENST00000373344.9:c.6325A>C	ENSP00000362441.4:p.Arg2109=
ENST00000395603.7:c.6211A>C	ENSP00000378967.3:p.Arg2071=
ENST00000480283.5:c.*5953A>C	ENSP00000480196.1:n.*5953A>C
ENST00000623706.3:n.3395A>C
NM_000489.4:c.6325A>C	NP_000480.3:p.Arg2109=
NM_138270.3:c.6211A>C	NP_612114.2:p.Arg2071=
XM_005262153.3:c.6322A>C	XP_005262210.2:p.Arg2108=
XM_005262154.3:c.6238A>C	XP_005262211.2:p.Arg2080=
XM_005262155.3:c.6208A>C	XP_005262212.2:p.Arg2070=
XM_005262156.3:c.6160A>C	XP_005262213.2:p.Arg2054=
XM_005262157.3:c.6121A>C	XP_005262214.2:p.Arg2041=
XM_006724666.2:c.6208A>C	XP_006724729.1:p.Arg2070=
XM_006724667.2:c.6046A>C	XP_006724730.1:p.Arg2016=
XR_938400.1:n.6667A>C
NM_000489.5:c.6325A>C	NP_000480.3:p.Arg2109=
XM_005262153.5:c.6322A>C	XP_005262210.2:p.Arg2108=
XM_005262154.5:c.6238A>C	XP_005262211.2:p.Arg2080=
XM_005262155.4:c.6208A>C	XP_005262212.2:p.Arg2070=
XM_005262156.4:c.6160A>C	XP_005262213.2:p.Arg2054=
XM_005262157.5:c.6121A>C	XP_005262214.2:p.Arg2041=
XM_006724666.4:c.6208A>C	XP_006724729.1:p.Arg2070=
XM_006724667.3:c.6046A>C	XP_006724730.1:p.Arg2016=
XM_017029601.2:c.6235A>C	XP_016885090.1:p.Arg2079=
XM_017029602.1:c.6205A>C	XP_016885091.1:p.Arg2069=
XM_017029603.1:c.6157A>C	XP_016885092.1:p.Arg2053=
XM_017029604.2:c.6124A>C	XP_016885093.1:p.Arg2042=
XM_017029605.1:c.6121A>C	XP_016885094.1:p.Arg2041=
XM_017029606.2:c.6094A>C	XP_016885095.1:p.Arg2032=
XM_017029607.2:c.6091A>C	XP_016885096.1:p.Arg2031=
XM_017029608.2:c.6043A>C	XP_016885097.1:p.Arg2015=
XM_017029609.1:c.6007A>C	XP_016885098.1:p.Arg2003=
XM_017029610.1:c.6004A>C	XP_016885099.1:p.Arg2002=
XM_017029611.1:c.5959A>C	XP_016885100.1:p.Arg1987=
XR_001755700.2:n.6624A>C
NM_138270.4:c.6211A>C	NP_612114.2:p.Arg2071=
NM_000489.6:c.6325A>C MANE Select	NP_000480.3:p.Arg2109=
NM_138270.5:c.6211A>C	NP_612114.2:p.Arg2071=