Canonical Allele Identifier: CA413704457

Gene: ATRX

Linked Data

• dbSNP Id: rs2147649767
• MyVariant Identifiers: chrX:g.76763987G>C (hg19) ; chrX:g.77508509G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7321C>G MANE Select	ENSP00000362441.4:p.Pro2441Ala
ENST00000675732.1:c.2419C>G	ENSP00000502598.1:p.Pro807Ala
ENST00000373344.9:c.7321C>G	ENSP00000362441.4:p.Pro2441Ala
ENST00000395603.7:c.7207C>G	ENSP00000378967.3:p.Pro2403Ala
ENST00000480283.5:c.*6949C>G	ENSP00000480196.1:n.*6949C>G
ENST00000623706.3:n.5641C>G
ENST00000624766.1:n.552C>G
NM_000489.4:c.7321C>G	NP_000480.3:p.Pro2441Ala
NM_138270.3:c.7207C>G	NP_612114.2:p.Pro2403Ala
XM_005262153.3:c.7318C>G	XP_005262210.2:p.Pro2440Ala
XM_005262154.3:c.7234C>G	XP_005262211.2:p.Pro2412Ala
XM_005262155.3:c.7204C>G	XP_005262212.2:p.Pro2402Ala
XM_005262156.3:c.7156C>G	XP_005262213.2:p.Pro2386Ala
XM_005262157.3:c.7117C>G	XP_005262214.2:p.Pro2373Ala
XM_006724666.2:c.7204C>G	XP_006724729.1:p.Pro2402Ala
XM_006724667.2:c.7042C>G	XP_006724730.1:p.Pro2348Ala
XR_938400.1:n.8913C>G
NM_000489.5:c.7321C>G	NP_000480.3:p.Pro2441Ala
XM_005262153.5:c.7318C>G	XP_005262210.2:p.Pro2440Ala
XM_005262154.5:c.7234C>G	XP_005262211.2:p.Pro2412Ala
XM_005262155.4:c.7204C>G	XP_005262212.2:p.Pro2402Ala
XM_005262156.4:c.7156C>G	XP_005262213.2:p.Pro2386Ala
XM_005262157.5:c.7117C>G	XP_005262214.2:p.Pro2373Ala
XM_006724666.4:c.7204C>G	XP_006724729.1:p.Pro2402Ala
XM_006724667.3:c.7042C>G	XP_006724730.1:p.Pro2348Ala
XM_017029601.2:c.7231C>G	XP_016885090.1:p.Pro2411Ala
XM_017029602.1:c.7201C>G	XP_016885091.1:p.Pro2401Ala
XM_017029603.1:c.7153C>G	XP_016885092.1:p.Pro2385Ala
XM_017029604.2:c.7120C>G	XP_016885093.1:p.Pro2374Ala
XM_017029605.1:c.7117C>G	XP_016885094.1:p.Pro2373Ala
XM_017029606.2:c.7090C>G	XP_016885095.1:p.Pro2364Ala
XM_017029607.2:c.7087C>G	XP_016885096.1:p.Pro2363Ala
XM_017029608.2:c.7039C>G	XP_016885097.1:p.Pro2347Ala
XM_017029609.1:c.7003C>G	XP_016885098.1:p.Pro2335Ala
XM_017029610.1:c.7000C>G	XP_016885099.1:p.Pro2334Ala
XM_017029611.1:c.6955C>G	XP_016885100.1:p.Pro2319Ala
XR_001755700.2:n.7620C>G
NM_138270.4:c.7207C>G	NP_612114.2:p.Pro2403Ala
NM_000489.6:c.7321C>G MANE Select	NP_000480.3:p.Pro2441Ala
NM_138270.5:c.7207C>G	NP_612114.2:p.Pro2403Ala