Canonical Allele Identifier: CA517374155

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76764012T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508534T>G , CM000685.2:g.77508534T>G	GRCh38
NC_000023.10:g.76764012T>G , CM000685.1:g.76764012T>G	GRCh37
NC_000023.9:g.76650668T>G	NCBI36
NG_008838.2:g.282688A>C
NG_008838.3:g.282736A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7296A>C MANE Select	ENSP00000362441.4:p.Thr2432=
ENST00000675732.1:c.2394A>C	ENSP00000502598.1:p.Thr798=
ENST00000373344.9:c.7296A>C	ENSP00000362441.4:p.Thr2432=
ENST00000395603.7:c.7182A>C	ENSP00000378967.3:p.Thr2394=
ENST00000480283.5:c.*6924A>C	ENSP00000480196.1:n.*6924A>C
ENST00000623706.3:n.5616A>C
ENST00000624766.1:n.527A>C
NM_000489.4:c.7296A>C	NP_000480.3:p.Thr2432=
NM_138270.3:c.7182A>C	NP_612114.2:p.Thr2394=
XM_005262153.3:c.7293A>C	XP_005262210.2:p.Thr2431=
XM_005262154.3:c.7209A>C	XP_005262211.2:p.Thr2403=
XM_005262155.3:c.7179A>C	XP_005262212.2:p.Thr2393=
XM_005262156.3:c.7131A>C	XP_005262213.2:p.Thr2377=
XM_005262157.3:c.7092A>C	XP_005262214.2:p.Thr2364=
XM_006724666.2:c.7179A>C	XP_006724729.1:p.Thr2393=
XM_006724667.2:c.7017A>C	XP_006724730.1:p.Thr2339=
XR_938400.1:n.8888A>C
NM_000489.5:c.7296A>C	NP_000480.3:p.Thr2432=
XM_005262153.5:c.7293A>C	XP_005262210.2:p.Thr2431=
XM_005262154.5:c.7209A>C	XP_005262211.2:p.Thr2403=
XM_005262155.4:c.7179A>C	XP_005262212.2:p.Thr2393=
XM_005262156.4:c.7131A>C	XP_005262213.2:p.Thr2377=
XM_005262157.5:c.7092A>C	XP_005262214.2:p.Thr2364=
XM_006724666.4:c.7179A>C	XP_006724729.1:p.Thr2393=
XM_006724667.3:c.7017A>C	XP_006724730.1:p.Thr2339=
XM_017029601.2:c.7206A>C	XP_016885090.1:p.Thr2402=
XM_017029602.1:c.7176A>C	XP_016885091.1:p.Thr2392=
XM_017029603.1:c.7128A>C	XP_016885092.1:p.Thr2376=
XM_017029604.2:c.7095A>C	XP_016885093.1:p.Thr2365=
XM_017029605.1:c.7092A>C	XP_016885094.1:p.Thr2364=
XM_017029606.2:c.7065A>C	XP_016885095.1:p.Thr2355=
XM_017029607.2:c.7062A>C	XP_016885096.1:p.Thr2354=
XM_017029608.2:c.7014A>C	XP_016885097.1:p.Thr2338=
XM_017029609.1:c.6978A>C	XP_016885098.1:p.Thr2326=
XM_017029610.1:c.6975A>C	XP_016885099.1:p.Thr2325=
XM_017029611.1:c.6930A>C	XP_016885100.1:p.Thr2310=
XR_001755700.2:n.7595A>C
NM_138270.4:c.7182A>C	NP_612114.2:p.Thr2394=
NM_000489.6:c.7296A>C MANE Select	NP_000480.3:p.Thr2432=
NM_138270.5:c.7182A>C	NP_612114.2:p.Thr2394=