Canonical Allele Identifier: CA413704661

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76764013G>T (hg19) ; chrX:g.77508535G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508535G>T , CM000685.2:g.77508535G>T	GRCh38
NC_000023.10:g.76764013G>T , CM000685.1:g.76764013G>T	GRCh37
NC_000023.9:g.76650669G>T	NCBI36
NG_008838.2:g.282687C>A
NG_008838.3:g.282735C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7295C>A MANE Select	ENSP00000362441.4:p.Thr2432Lys
ENST00000675732.1:c.2393C>A	ENSP00000502598.1:p.Thr798Lys
ENST00000373344.9:c.7295C>A	ENSP00000362441.4:p.Thr2432Lys
ENST00000395603.7:c.7181C>A	ENSP00000378967.3:p.Thr2394Lys
ENST00000480283.5:c.*6923C>A	ENSP00000480196.1:n.*6923C>A
ENST00000623706.3:n.5615C>A
ENST00000624766.1:n.526C>A
NM_000489.4:c.7295C>A	NP_000480.3:p.Thr2432Lys
NM_138270.3:c.7181C>A	NP_612114.2:p.Thr2394Lys
XM_005262153.3:c.7292C>A	XP_005262210.2:p.Thr2431Lys
XM_005262154.3:c.7208C>A	XP_005262211.2:p.Thr2403Lys
XM_005262155.3:c.7178C>A	XP_005262212.2:p.Thr2393Lys
XM_005262156.3:c.7130C>A	XP_005262213.2:p.Thr2377Lys
XM_005262157.3:c.7091C>A	XP_005262214.2:p.Thr2364Lys
XM_006724666.2:c.7178C>A	XP_006724729.1:p.Thr2393Lys
XM_006724667.2:c.7016C>A	XP_006724730.1:p.Thr2339Lys
XR_938400.1:n.8887C>A
NM_000489.5:c.7295C>A	NP_000480.3:p.Thr2432Lys
XM_005262153.5:c.7292C>A	XP_005262210.2:p.Thr2431Lys
XM_005262154.5:c.7208C>A	XP_005262211.2:p.Thr2403Lys
XM_005262155.4:c.7178C>A	XP_005262212.2:p.Thr2393Lys
XM_005262156.4:c.7130C>A	XP_005262213.2:p.Thr2377Lys
XM_005262157.5:c.7091C>A	XP_005262214.2:p.Thr2364Lys
XM_006724666.4:c.7178C>A	XP_006724729.1:p.Thr2393Lys
XM_006724667.3:c.7016C>A	XP_006724730.1:p.Thr2339Lys
XM_017029601.2:c.7205C>A	XP_016885090.1:p.Thr2402Lys
XM_017029602.1:c.7175C>A	XP_016885091.1:p.Thr2392Lys
XM_017029603.1:c.7127C>A	XP_016885092.1:p.Thr2376Lys
XM_017029604.2:c.7094C>A	XP_016885093.1:p.Thr2365Lys
XM_017029605.1:c.7091C>A	XP_016885094.1:p.Thr2364Lys
XM_017029606.2:c.7064C>A	XP_016885095.1:p.Thr2355Lys
XM_017029607.2:c.7061C>A	XP_016885096.1:p.Thr2354Lys
XM_017029608.2:c.7013C>A	XP_016885097.1:p.Thr2338Lys
XM_017029609.1:c.6977C>A	XP_016885098.1:p.Thr2326Lys
XM_017029610.1:c.6974C>A	XP_016885099.1:p.Thr2325Lys
XM_017029611.1:c.6929C>A	XP_016885100.1:p.Thr2310Lys
XR_001755700.2:n.7594C>A
NM_138270.4:c.7181C>A	NP_612114.2:p.Thr2394Lys
NM_000489.6:c.7295C>A MANE Select	NP_000480.3:p.Thr2432Lys
NM_138270.5:c.7181C>A	NP_612114.2:p.Thr2394Lys