Canonical Allele Identifier: CA517374830

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829806G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574341G>T , CM000685.2:g.77574341G>T	GRCh38
NC_000023.10:g.76829806G>T , CM000685.1:g.76829806G>T	GRCh37
NC_000023.9:g.76716462G>T	NCBI36
NG_008838.2:g.216881C>A
NG_008838.3:g.216929C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6235C>A MANE Select	ENSP00000362441.4:p.Arg2079=
ENST00000636152.1:n.70C>A
ENST00000675732.1:c.1333C>A	ENSP00000502598.1:p.Arg445=
ENST00000373344.9:c.6235C>A	ENSP00000362441.4:p.Arg2079=
ENST00000395603.7:c.6121C>A	ENSP00000378967.3:p.Arg2041=
ENST00000480283.5:c.*5863C>A	ENSP00000480196.1:n.*5863C>A
ENST00000623316.1:c.719C>A
ENST00000623706.3:n.3305C>A
NM_000489.4:c.6235C>A	NP_000480.3:p.Arg2079=
NM_138270.3:c.6121C>A	NP_612114.2:p.Arg2041=
XM_005262153.3:c.6232C>A	XP_005262210.2:p.Arg2078=
XM_005262154.3:c.6148C>A	XP_005262211.2:p.Arg2050=
XM_005262155.3:c.6118C>A	XP_005262212.2:p.Arg2040=
XM_005262156.3:c.6070C>A	XP_005262213.2:p.Arg2024=
XM_005262157.3:c.6031C>A	XP_005262214.2:p.Arg2011=
XM_006724666.2:c.6118C>A	XP_006724729.1:p.Arg2040=
XM_006724667.2:c.5956C>A	XP_006724730.1:p.Arg1986=
XR_938400.1:n.6577C>A
NM_000489.5:c.6235C>A	NP_000480.3:p.Arg2079=
XM_005262153.5:c.6232C>A	XP_005262210.2:p.Arg2078=
XM_005262154.5:c.6148C>A	XP_005262211.2:p.Arg2050=
XM_005262155.4:c.6118C>A	XP_005262212.2:p.Arg2040=
XM_005262156.4:c.6070C>A	XP_005262213.2:p.Arg2024=
XM_005262157.5:c.6031C>A	XP_005262214.2:p.Arg2011=
XM_006724666.4:c.6118C>A	XP_006724729.1:p.Arg2040=
XM_006724667.3:c.5956C>A	XP_006724730.1:p.Arg1986=
XM_017029601.2:c.6145C>A	XP_016885090.1:p.Arg2049=
XM_017029602.1:c.6115C>A	XP_016885091.1:p.Arg2039=
XM_017029603.1:c.6067C>A	XP_016885092.1:p.Arg2023=
XM_017029604.2:c.6034C>A	XP_016885093.1:p.Arg2012=
XM_017029605.1:c.6031C>A	XP_016885094.1:p.Arg2011=
XM_017029606.2:c.6004C>A	XP_016885095.1:p.Arg2002=
XM_017029607.2:c.6001C>A	XP_016885096.1:p.Arg2001=
XM_017029608.2:c.5953C>A	XP_016885097.1:p.Arg1985=
XM_017029609.1:c.5917C>A	XP_016885098.1:p.Arg1973=
XM_017029610.1:c.5914C>A	XP_016885099.1:p.Arg1972=
XM_017029611.1:c.5869C>A	XP_016885100.1:p.Arg1957=
XR_001755700.2:n.6534C>A
NM_138270.4:c.6121C>A	NP_612114.2:p.Arg2041=
NM_000489.6:c.6235C>A MANE Select	NP_000480.3:p.Arg2079=
NM_138270.5:c.6121C>A	NP_612114.2:p.Arg2041=