Canonical Allele Identifier: CA517374165

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76764027A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508549A>C , CM000685.2:g.77508549A>C	GRCh38
NC_000023.10:g.76764027A>C , CM000685.1:g.76764027A>C	GRCh37
NC_000023.9:g.76650683A>C	NCBI36
NG_008838.2:g.282673T>G
NG_008838.3:g.282721T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7281T>G MANE Select	ENSP00000362441.4:p.Thr2427=
ENST00000675732.1:c.2379T>G	ENSP00000502598.1:p.Thr793=
ENST00000373344.9:c.7281T>G	ENSP00000362441.4:p.Thr2427=
ENST00000395603.7:c.7167T>G	ENSP00000378967.3:p.Thr2389=
ENST00000480283.5:c.*6909T>G	ENSP00000480196.1:n.*6909T>G
ENST00000623706.3:n.5601T>G
ENST00000624766.1:n.512T>G
NM_000489.4:c.7281T>G	NP_000480.3:p.Thr2427=
NM_138270.3:c.7167T>G	NP_612114.2:p.Thr2389=
XM_005262153.3:c.7278T>G	XP_005262210.2:p.Thr2426=
XM_005262154.3:c.7194T>G	XP_005262211.2:p.Thr2398=
XM_005262155.3:c.7164T>G	XP_005262212.2:p.Thr2388=
XM_005262156.3:c.7116T>G	XP_005262213.2:p.Thr2372=
XM_005262157.3:c.7077T>G	XP_005262214.2:p.Thr2359=
XM_006724666.2:c.7164T>G	XP_006724729.1:p.Thr2388=
XM_006724667.2:c.7002T>G	XP_006724730.1:p.Thr2334=
XR_938400.1:n.8873T>G
NM_000489.5:c.7281T>G	NP_000480.3:p.Thr2427=
XM_005262153.5:c.7278T>G	XP_005262210.2:p.Thr2426=
XM_005262154.5:c.7194T>G	XP_005262211.2:p.Thr2398=
XM_005262155.4:c.7164T>G	XP_005262212.2:p.Thr2388=
XM_005262156.4:c.7116T>G	XP_005262213.2:p.Thr2372=
XM_005262157.5:c.7077T>G	XP_005262214.2:p.Thr2359=
XM_006724666.4:c.7164T>G	XP_006724729.1:p.Thr2388=
XM_006724667.3:c.7002T>G	XP_006724730.1:p.Thr2334=
XM_017029601.2:c.7191T>G	XP_016885090.1:p.Thr2397=
XM_017029602.1:c.7161T>G	XP_016885091.1:p.Thr2387=
XM_017029603.1:c.7113T>G	XP_016885092.1:p.Thr2371=
XM_017029604.2:c.7080T>G	XP_016885093.1:p.Thr2360=
XM_017029605.1:c.7077T>G	XP_016885094.1:p.Thr2359=
XM_017029606.2:c.7050T>G	XP_016885095.1:p.Thr2350=
XM_017029607.2:c.7047T>G	XP_016885096.1:p.Thr2349=
XM_017029608.2:c.6999T>G	XP_016885097.1:p.Thr2333=
XM_017029609.1:c.6963T>G	XP_016885098.1:p.Thr2321=
XM_017029610.1:c.6960T>G	XP_016885099.1:p.Thr2320=
XM_017029611.1:c.6915T>G	XP_016885100.1:p.Thr2305=
XR_001755700.2:n.7580T>G
NM_138270.4:c.7167T>G	NP_612114.2:p.Thr2389=
NM_000489.6:c.7281T>G MANE Select	NP_000480.3:p.Thr2427=
NM_138270.5:c.7167T>G	NP_612114.2:p.Thr2389=