Canonical Allele Identifier: CA517374791

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829774G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574309G>T , CM000685.2:g.77574309G>T	GRCh38
NC_000023.10:g.76829774G>T , CM000685.1:g.76829774G>T	GRCh37
NC_000023.9:g.76716430G>T	NCBI36
NG_008838.2:g.216913C>A
NG_008838.3:g.216961C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6267C>A MANE Select	ENSP00000362441.4:p.Ser2089=
ENST00000675732.1:c.1365C>A	ENSP00000502598.1:p.Ser455=
ENST00000373344.9:c.6267C>A	ENSP00000362441.4:p.Ser2089=
ENST00000395603.7:c.6153C>A	ENSP00000378967.3:p.Ser2051=
ENST00000480283.5:c.*5895C>A	ENSP00000480196.1:n.*5895C>A
ENST00000623316.1:c.751C>A
ENST00000623706.3:n.3337C>A
NM_000489.4:c.6267C>A	NP_000480.3:p.Ser2089=
NM_138270.3:c.6153C>A	NP_612114.2:p.Ser2051=
XM_005262153.3:c.6264C>A	XP_005262210.2:p.Ser2088=
XM_005262154.3:c.6180C>A	XP_005262211.2:p.Ser2060=
XM_005262155.3:c.6150C>A	XP_005262212.2:p.Ser2050=
XM_005262156.3:c.6102C>A	XP_005262213.2:p.Ser2034=
XM_005262157.3:c.6063C>A	XP_005262214.2:p.Ser2021=
XM_006724666.2:c.6150C>A	XP_006724729.1:p.Ser2050=
XM_006724667.2:c.5988C>A	XP_006724730.1:p.Ser1996=
XR_938400.1:n.6609C>A
NM_000489.5:c.6267C>A	NP_000480.3:p.Ser2089=
XM_005262153.5:c.6264C>A	XP_005262210.2:p.Ser2088=
XM_005262154.5:c.6180C>A	XP_005262211.2:p.Ser2060=
XM_005262155.4:c.6150C>A	XP_005262212.2:p.Ser2050=
XM_005262156.4:c.6102C>A	XP_005262213.2:p.Ser2034=
XM_005262157.5:c.6063C>A	XP_005262214.2:p.Ser2021=
XM_006724666.4:c.6150C>A	XP_006724729.1:p.Ser2050=
XM_006724667.3:c.5988C>A	XP_006724730.1:p.Ser1996=
XM_017029601.2:c.6177C>A	XP_016885090.1:p.Ser2059=
XM_017029602.1:c.6147C>A	XP_016885091.1:p.Ser2049=
XM_017029603.1:c.6099C>A	XP_016885092.1:p.Ser2033=
XM_017029604.2:c.6066C>A	XP_016885093.1:p.Ser2022=
XM_017029605.1:c.6063C>A	XP_016885094.1:p.Ser2021=
XM_017029606.2:c.6036C>A	XP_016885095.1:p.Ser2012=
XM_017029607.2:c.6033C>A	XP_016885096.1:p.Ser2011=
XM_017029608.2:c.5985C>A	XP_016885097.1:p.Ser1995=
XM_017029609.1:c.5949C>A	XP_016885098.1:p.Ser1983=
XM_017029610.1:c.5946C>A	XP_016885099.1:p.Ser1982=
XM_017029611.1:c.5901C>A	XP_016885100.1:p.Ser1967=
XR_001755700.2:n.6566C>A
NM_138270.4:c.6153C>A	NP_612114.2:p.Ser2051=
NM_000489.6:c.6267C>A MANE Select	NP_000480.3:p.Ser2089=
NM_138270.5:c.6153C>A	NP_612114.2:p.Ser2051=