Canonical Allele Identifier: CA517471444

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907682T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652192T>C , CM000685.2:g.77652192T>C	GRCh38
NC_000023.10:g.76907682T>C , CM000685.1:g.76907682T>C	GRCh37
NC_000023.9:g.76794338T>C	NCBI36
NG_008838.2:g.139030A>G
NG_008838.3:g.139078A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4479A>G MANE Select	ENSP00000362441.4:p.Thr1493=
ENST00000373344.9:c.4479A>G	ENSP00000362441.4:p.Thr1493=
ENST00000395603.7:c.4365A>G	ENSP00000378967.3:p.Thr1455=
ENST00000480283.5:c.*4107A>G	ENSP00000480196.1:n.*4107A>G
ENST00000623242.3:c.85A>G
NM_000489.4:c.4479A>G	NP_000480.3:p.Thr1493=
NM_138270.3:c.4365A>G	NP_612114.2:p.Thr1455=
XM_005262153.3:c.4476A>G	XP_005262210.2:p.Thr1492=
XM_005262154.3:c.4392A>G	XP_005262211.2:p.Thr1464=
XM_005262155.3:c.4362A>G	XP_005262212.2:p.Thr1454=
XM_005262156.3:c.4314A>G	XP_005262213.2:p.Thr1438=
XM_005262157.3:c.4275A>G	XP_005262214.2:p.Thr1425=
XM_006724666.2:c.4362A>G	XP_006724729.1:p.Thr1454=
XM_006724667.2:c.4200A>G	XP_006724730.1:p.Thr1400=
XM_006724668.2:c.4479A>G	XP_006724731.1:p.Thr1493=
XR_938400.1:n.4747A>G
NM_000489.5:c.4479A>G	NP_000480.3:p.Thr1493=
XM_005262153.5:c.4476A>G	XP_005262210.2:p.Thr1492=
XM_005262154.5:c.4392A>G	XP_005262211.2:p.Thr1464=
XM_005262155.4:c.4362A>G	XP_005262212.2:p.Thr1454=
XM_005262156.4:c.4314A>G	XP_005262213.2:p.Thr1438=
XM_005262157.5:c.4275A>G	XP_005262214.2:p.Thr1425=
XM_006724666.4:c.4362A>G	XP_006724729.1:p.Thr1454=
XM_006724667.3:c.4200A>G	XP_006724730.1:p.Thr1400=
XM_006724668.3:c.4479A>G	XP_006724731.1:p.Thr1493=
XM_017029601.2:c.4389A>G	XP_016885090.1:p.Thr1463=
XM_017029602.1:c.4359A>G	XP_016885091.1:p.Thr1453=
XM_017029603.1:c.4311A>G	XP_016885092.1:p.Thr1437=
XM_017029604.2:c.4278A>G	XP_016885093.1:p.Thr1426=
XM_017029605.1:c.4275A>G	XP_016885094.1:p.Thr1425=
XM_017029606.2:c.4248A>G	XP_016885095.1:p.Thr1416=
XM_017029607.2:c.4245A>G	XP_016885096.1:p.Thr1415=
XM_017029608.2:c.4197A>G	XP_016885097.1:p.Thr1399=
XM_017029609.1:c.4161A>G	XP_016885098.1:p.Thr1387=
XM_017029610.1:c.4158A>G	XP_016885099.1:p.Thr1386=
XM_017029611.1:c.4113A>G	XP_016885100.1:p.Thr1371=
XR_001755700.2:n.4704A>G
NM_138270.4:c.4365A>G	NP_612114.2:p.Thr1455=
NM_000489.6:c.4479A>G MANE Select	NP_000480.3:p.Thr1493=
NM_138270.5:c.4365A>G	NP_612114.2:p.Thr1455=