Canonical Allele Identifier: CA413704454

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763987G>T (hg19) ; chrX:g.77508509G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508509G>T , CM000685.2:g.77508509G>T	GRCh38
NC_000023.10:g.76763987G>T , CM000685.1:g.76763987G>T	GRCh37
NC_000023.9:g.76650643G>T	NCBI36
NG_008838.2:g.282713C>A
NG_008838.3:g.282761C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7321C>A MANE Select	ENSP00000362441.4:p.Pro2441Thr
ENST00000675732.1:c.2419C>A	ENSP00000502598.1:p.Pro807Thr
ENST00000373344.9:c.7321C>A	ENSP00000362441.4:p.Pro2441Thr
ENST00000395603.7:c.7207C>A	ENSP00000378967.3:p.Pro2403Thr
ENST00000480283.5:c.*6949C>A	ENSP00000480196.1:n.*6949C>A
ENST00000623706.3:n.5641C>A
ENST00000624766.1:n.552C>A
NM_000489.4:c.7321C>A	NP_000480.3:p.Pro2441Thr
NM_138270.3:c.7207C>A	NP_612114.2:p.Pro2403Thr
XM_005262153.3:c.7318C>A	XP_005262210.2:p.Pro2440Thr
XM_005262154.3:c.7234C>A	XP_005262211.2:p.Pro2412Thr
XM_005262155.3:c.7204C>A	XP_005262212.2:p.Pro2402Thr
XM_005262156.3:c.7156C>A	XP_005262213.2:p.Pro2386Thr
XM_005262157.3:c.7117C>A	XP_005262214.2:p.Pro2373Thr
XM_006724666.2:c.7204C>A	XP_006724729.1:p.Pro2402Thr
XM_006724667.2:c.7042C>A	XP_006724730.1:p.Pro2348Thr
XR_938400.1:n.8913C>A
NM_000489.5:c.7321C>A	NP_000480.3:p.Pro2441Thr
XM_005262153.5:c.7318C>A	XP_005262210.2:p.Pro2440Thr
XM_005262154.5:c.7234C>A	XP_005262211.2:p.Pro2412Thr
XM_005262155.4:c.7204C>A	XP_005262212.2:p.Pro2402Thr
XM_005262156.4:c.7156C>A	XP_005262213.2:p.Pro2386Thr
XM_005262157.5:c.7117C>A	XP_005262214.2:p.Pro2373Thr
XM_006724666.4:c.7204C>A	XP_006724729.1:p.Pro2402Thr
XM_006724667.3:c.7042C>A	XP_006724730.1:p.Pro2348Thr
XM_017029601.2:c.7231C>A	XP_016885090.1:p.Pro2411Thr
XM_017029602.1:c.7201C>A	XP_016885091.1:p.Pro2401Thr
XM_017029603.1:c.7153C>A	XP_016885092.1:p.Pro2385Thr
XM_017029604.2:c.7120C>A	XP_016885093.1:p.Pro2374Thr
XM_017029605.1:c.7117C>A	XP_016885094.1:p.Pro2373Thr
XM_017029606.2:c.7090C>A	XP_016885095.1:p.Pro2364Thr
XM_017029607.2:c.7087C>A	XP_016885096.1:p.Pro2363Thr
XM_017029608.2:c.7039C>A	XP_016885097.1:p.Pro2347Thr
XM_017029609.1:c.7003C>A	XP_016885098.1:p.Pro2335Thr
XM_017029610.1:c.7000C>A	XP_016885099.1:p.Pro2334Thr
XM_017029611.1:c.6955C>A	XP_016885100.1:p.Pro2319Thr
XR_001755700.2:n.7620C>A
NM_138270.4:c.7207C>A	NP_612114.2:p.Pro2403Thr
NM_000489.6:c.7321C>A MANE Select	NP_000480.3:p.Pro2441Thr
NM_138270.5:c.7207C>A	NP_612114.2:p.Pro2403Thr