Canonical Allele Identifier: CA517374826

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829804T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574339T>G , CM000685.2:g.77574339T>G	GRCh38
NC_000023.10:g.76829804T>G , CM000685.1:g.76829804T>G	GRCh37
NC_000023.9:g.76716460T>G	NCBI36
NG_008838.2:g.216883A>C
NG_008838.3:g.216931A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000373344.11:c.6237A>C MANE Select	ENSP00000362441.4:p.Arg2079=
ENST00000636152.1:n.72A>C
ENST00000675732.1:c.1335A>C	ENSP00000502598.1:p.Arg445=
ENST00000373344.9:c.6237A>C	ENSP00000362441.4:p.Arg2079=
ENST00000395603.7:c.6123A>C	ENSP00000378967.3:p.Arg2041=
ENST00000480283.5:c.*5865A>C	ENSP00000480196.1:n.*5865A>C
ENST00000623316.1:c.721A>C
ENST00000623706.3:n.3307A>C
NM_000489.4:c.6237A>C	NP_000480.3:p.Arg2079=
NM_138270.3:c.6123A>C	NP_612114.2:p.Arg2041=
XM_005262153.3:c.6234A>C	XP_005262210.2:p.Arg2078=
XM_005262154.3:c.6150A>C	XP_005262211.2:p.Arg2050=
XM_005262155.3:c.6120A>C	XP_005262212.2:p.Arg2040=
XM_005262156.3:c.6072A>C	XP_005262213.2:p.Arg2024=
XM_005262157.3:c.6033A>C	XP_005262214.2:p.Arg2011=
XM_006724666.2:c.6120A>C	XP_006724729.1:p.Arg2040=
XM_006724667.2:c.5958A>C	XP_006724730.1:p.Arg1986=
XR_938400.1:n.6579A>C
NM_000489.5:c.6237A>C	NP_000480.3:p.Arg2079=
XM_005262153.5:c.6234A>C	XP_005262210.2:p.Arg2078=
XM_005262154.5:c.6150A>C	XP_005262211.2:p.Arg2050=
XM_005262155.4:c.6120A>C	XP_005262212.2:p.Arg2040=
XM_005262156.4:c.6072A>C	XP_005262213.2:p.Arg2024=
XM_005262157.5:c.6033A>C	XP_005262214.2:p.Arg2011=
XM_006724666.4:c.6120A>C	XP_006724729.1:p.Arg2040=
XM_006724667.3:c.5958A>C	XP_006724730.1:p.Arg1986=
XM_017029601.2:c.6147A>C	XP_016885090.1:p.Arg2049=
XM_017029602.1:c.6117A>C	XP_016885091.1:p.Arg2039=
XM_017029603.1:c.6069A>C	XP_016885092.1:p.Arg2023=
XM_017029604.2:c.6036A>C	XP_016885093.1:p.Arg2012=
XM_017029605.1:c.6033A>C	XP_016885094.1:p.Arg2011=
XM_017029606.2:c.6006A>C	XP_016885095.1:p.Arg2002=
XM_017029607.2:c.6003A>C	XP_016885096.1:p.Arg2001=
XM_017029608.2:c.5955A>C	XP_016885097.1:p.Arg1985=
XM_017029609.1:c.5919A>C	XP_016885098.1:p.Arg1973=
XM_017029610.1:c.5916A>C	XP_016885099.1:p.Arg1972=
XM_017029611.1:c.5871A>C	XP_016885100.1:p.Arg1957=
XR_001755700.2:n.6536A>C
NM_138270.4:c.6123A>C	NP_612114.2:p.Arg2041=
NM_000489.6:c.6237A>C MANE Select	NP_000480.3:p.Arg2079=
NM_138270.5:c.6123A>C	NP_612114.2:p.Arg2041=