Canonical Allele Identifier: CA517374748

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829723A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574258A>C , CM000685.2:g.77574258A>C	GRCh38
NC_000023.10:g.76829723A>C , CM000685.1:g.76829723A>C	GRCh37
NC_000023.9:g.76716379A>C	NCBI36
NG_008838.2:g.216964T>G
NG_008838.3:g.217012T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6318T>G MANE Select	ENSP00000362441.4:p.Thr2106=
ENST00000675732.1:c.1416T>G	ENSP00000502598.1:p.Thr472=
ENST00000373344.9:c.6318T>G	ENSP00000362441.4:p.Thr2106=
ENST00000395603.7:c.6204T>G	ENSP00000378967.3:p.Thr2068=
ENST00000480283.5:c.*5946T>G	ENSP00000480196.1:n.*5946T>G
ENST00000623316.1:c.802T>G
ENST00000623706.3:n.3388T>G
NM_000489.4:c.6318T>G	NP_000480.3:p.Thr2106=
NM_138270.3:c.6204T>G	NP_612114.2:p.Thr2068=
XM_005262153.3:c.6315T>G	XP_005262210.2:p.Thr2105=
XM_005262154.3:c.6231T>G	XP_005262211.2:p.Thr2077=
XM_005262155.3:c.6201T>G	XP_005262212.2:p.Thr2067=
XM_005262156.3:c.6153T>G	XP_005262213.2:p.Thr2051=
XM_005262157.3:c.6114T>G	XP_005262214.2:p.Thr2038=
XM_006724666.2:c.6201T>G	XP_006724729.1:p.Thr2067=
XM_006724667.2:c.6039T>G	XP_006724730.1:p.Thr2013=
XR_938400.1:n.6660T>G
NM_000489.5:c.6318T>G	NP_000480.3:p.Thr2106=
XM_005262153.5:c.6315T>G	XP_005262210.2:p.Thr2105=
XM_005262154.5:c.6231T>G	XP_005262211.2:p.Thr2077=
XM_005262155.4:c.6201T>G	XP_005262212.2:p.Thr2067=
XM_005262156.4:c.6153T>G	XP_005262213.2:p.Thr2051=
XM_005262157.5:c.6114T>G	XP_005262214.2:p.Thr2038=
XM_006724666.4:c.6201T>G	XP_006724729.1:p.Thr2067=
XM_006724667.3:c.6039T>G	XP_006724730.1:p.Thr2013=
XM_017029601.2:c.6228T>G	XP_016885090.1:p.Thr2076=
XM_017029602.1:c.6198T>G	XP_016885091.1:p.Thr2066=
XM_017029603.1:c.6150T>G	XP_016885092.1:p.Thr2050=
XM_017029604.2:c.6117T>G	XP_016885093.1:p.Thr2039=
XM_017029605.1:c.6114T>G	XP_016885094.1:p.Thr2038=
XM_017029606.2:c.6087T>G	XP_016885095.1:p.Thr2029=
XM_017029607.2:c.6084T>G	XP_016885096.1:p.Thr2028=
XM_017029608.2:c.6036T>G	XP_016885097.1:p.Thr2012=
XM_017029609.1:c.6000T>G	XP_016885098.1:p.Thr2000=
XM_017029610.1:c.5997T>G	XP_016885099.1:p.Thr1999=
XM_017029611.1:c.5952T>G	XP_016885100.1:p.Thr1984=
XR_001755700.2:n.6617T>G
NM_138270.4:c.6204T>G	NP_612114.2:p.Thr2068=
NM_000489.6:c.6318T>G MANE Select	NP_000480.3:p.Thr2106=
NM_138270.5:c.6204T>G	NP_612114.2:p.Thr2068=