Canonical Allele Identifier: CA517374787

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829771A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574306A>T , CM000685.2:g.77574306A>T	GRCh38
NC_000023.10:g.76829771A>T , CM000685.1:g.76829771A>T	GRCh37
NC_000023.9:g.76716427A>T	NCBI36
NG_008838.2:g.216916T>A
NG_008838.3:g.216964T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6270T>A MANE Select	ENSP00000362441.4:p.Thr2090=
ENST00000675732.1:c.1368T>A	ENSP00000502598.1:p.Thr456=
ENST00000373344.9:c.6270T>A	ENSP00000362441.4:p.Thr2090=
ENST00000395603.7:c.6156T>A	ENSP00000378967.3:p.Thr2052=
ENST00000480283.5:c.*5898T>A	ENSP00000480196.1:n.*5898T>A
ENST00000623316.1:c.754T>A
ENST00000623706.3:n.3340T>A
NM_000489.4:c.6270T>A	NP_000480.3:p.Thr2090=
NM_138270.3:c.6156T>A	NP_612114.2:p.Thr2052=
XM_005262153.3:c.6267T>A	XP_005262210.2:p.Thr2089=
XM_005262154.3:c.6183T>A	XP_005262211.2:p.Thr2061=
XM_005262155.3:c.6153T>A	XP_005262212.2:p.Thr2051=
XM_005262156.3:c.6105T>A	XP_005262213.2:p.Thr2035=
XM_005262157.3:c.6066T>A	XP_005262214.2:p.Thr2022=
XM_006724666.2:c.6153T>A	XP_006724729.1:p.Thr2051=
XM_006724667.2:c.5991T>A	XP_006724730.1:p.Thr1997=
XR_938400.1:n.6612T>A
NM_000489.5:c.6270T>A	NP_000480.3:p.Thr2090=
XM_005262153.5:c.6267T>A	XP_005262210.2:p.Thr2089=
XM_005262154.5:c.6183T>A	XP_005262211.2:p.Thr2061=
XM_005262155.4:c.6153T>A	XP_005262212.2:p.Thr2051=
XM_005262156.4:c.6105T>A	XP_005262213.2:p.Thr2035=
XM_005262157.5:c.6066T>A	XP_005262214.2:p.Thr2022=
XM_006724666.4:c.6153T>A	XP_006724729.1:p.Thr2051=
XM_006724667.3:c.5991T>A	XP_006724730.1:p.Thr1997=
XM_017029601.2:c.6180T>A	XP_016885090.1:p.Thr2060=
XM_017029602.1:c.6150T>A	XP_016885091.1:p.Thr2050=
XM_017029603.1:c.6102T>A	XP_016885092.1:p.Thr2034=
XM_017029604.2:c.6069T>A	XP_016885093.1:p.Thr2023=
XM_017029605.1:c.6066T>A	XP_016885094.1:p.Thr2022=
XM_017029606.2:c.6039T>A	XP_016885095.1:p.Thr2013=
XM_017029607.2:c.6036T>A	XP_016885096.1:p.Thr2012=
XM_017029608.2:c.5988T>A	XP_016885097.1:p.Thr1996=
XM_017029609.1:c.5952T>A	XP_016885098.1:p.Thr1984=
XM_017029610.1:c.5949T>A	XP_016885099.1:p.Thr1983=
XM_017029611.1:c.5904T>A	XP_016885100.1:p.Thr1968=
XR_001755700.2:n.6569T>A
NM_138270.4:c.6156T>A	NP_612114.2:p.Thr2052=
NM_000489.6:c.6270T>A MANE Select	NP_000480.3:p.Thr2090=
NM_138270.5:c.6156T>A	NP_612114.2:p.Thr2052=