Canonical Allele Identifier: CA413704656

Gene: ATRX

Linked Data

• dbSNP Id: rs2147650760
• MyVariant Identifiers: chrX:g.76764013G>C (hg19) ; chrX:g.77508535G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7295C>G MANE Select	ENSP00000362441.4:p.Thr2432Arg
ENST00000675732.1:c.2393C>G	ENSP00000502598.1:p.Thr798Arg
ENST00000373344.9:c.7295C>G	ENSP00000362441.4:p.Thr2432Arg
ENST00000395603.7:c.7181C>G	ENSP00000378967.3:p.Thr2394Arg
ENST00000480283.5:c.*6923C>G	ENSP00000480196.1:n.*6923C>G
ENST00000623706.3:n.5615C>G
ENST00000624766.1:n.526C>G
NM_000489.4:c.7295C>G	NP_000480.3:p.Thr2432Arg
NM_138270.3:c.7181C>G	NP_612114.2:p.Thr2394Arg
XM_005262153.3:c.7292C>G	XP_005262210.2:p.Thr2431Arg
XM_005262154.3:c.7208C>G	XP_005262211.2:p.Thr2403Arg
XM_005262155.3:c.7178C>G	XP_005262212.2:p.Thr2393Arg
XM_005262156.3:c.7130C>G	XP_005262213.2:p.Thr2377Arg
XM_005262157.3:c.7091C>G	XP_005262214.2:p.Thr2364Arg
XM_006724666.2:c.7178C>G	XP_006724729.1:p.Thr2393Arg
XM_006724667.2:c.7016C>G	XP_006724730.1:p.Thr2339Arg
XR_938400.1:n.8887C>G
NM_000489.5:c.7295C>G	NP_000480.3:p.Thr2432Arg
XM_005262153.5:c.7292C>G	XP_005262210.2:p.Thr2431Arg
XM_005262154.5:c.7208C>G	XP_005262211.2:p.Thr2403Arg
XM_005262155.4:c.7178C>G	XP_005262212.2:p.Thr2393Arg
XM_005262156.4:c.7130C>G	XP_005262213.2:p.Thr2377Arg
XM_005262157.5:c.7091C>G	XP_005262214.2:p.Thr2364Arg
XM_006724666.4:c.7178C>G	XP_006724729.1:p.Thr2393Arg
XM_006724667.3:c.7016C>G	XP_006724730.1:p.Thr2339Arg
XM_017029601.2:c.7205C>G	XP_016885090.1:p.Thr2402Arg
XM_017029602.1:c.7175C>G	XP_016885091.1:p.Thr2392Arg
XM_017029603.1:c.7127C>G	XP_016885092.1:p.Thr2376Arg
XM_017029604.2:c.7094C>G	XP_016885093.1:p.Thr2365Arg
XM_017029605.1:c.7091C>G	XP_016885094.1:p.Thr2364Arg
XM_017029606.2:c.7064C>G	XP_016885095.1:p.Thr2355Arg
XM_017029607.2:c.7061C>G	XP_016885096.1:p.Thr2354Arg
XM_017029608.2:c.7013C>G	XP_016885097.1:p.Thr2338Arg
XM_017029609.1:c.6977C>G	XP_016885098.1:p.Thr2326Arg
XM_017029610.1:c.6974C>G	XP_016885099.1:p.Thr2325Arg
XM_017029611.1:c.6929C>G	XP_016885100.1:p.Thr2310Arg
XR_001755700.2:n.7594C>G
NM_138270.4:c.7181C>G	NP_612114.2:p.Thr2394Arg
NM_000489.6:c.7295C>G MANE Select	NP_000480.3:p.Thr2432Arg
NM_138270.5:c.7181C>G	NP_612114.2:p.Thr2394Arg