Canonical Allele Identifier: CA413700858

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829722T>C (hg19) ; chrX:g.77574257T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574257T>C , CM000685.2:g.77574257T>C	GRCh38
NC_000023.10:g.76829722T>C , CM000685.1:g.76829722T>C	GRCh37
NC_000023.9:g.76716378T>C	NCBI36
NG_008838.2:g.216965A>G
NG_008838.3:g.217013A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6319A>G MANE Select	ENSP00000362441.4:p.Asn2107Asp
ENST00000675732.1:c.1417A>G	ENSP00000502598.1:p.Asn473Asp
ENST00000373344.9:c.6319A>G	ENSP00000362441.4:p.Asn2107Asp
ENST00000395603.7:c.6205A>G	ENSP00000378967.3:p.Asn2069Asp
ENST00000480283.5:c.*5947A>G	ENSP00000480196.1:n.*5947A>G
ENST00000623316.1:c.803A>G
ENST00000623706.3:n.3389A>G
NM_000489.4:c.6319A>G	NP_000480.3:p.Asn2107Asp
NM_138270.3:c.6205A>G	NP_612114.2:p.Asn2069Asp
XM_005262153.3:c.6316A>G	XP_005262210.2:p.Asn2106Asp
XM_005262154.3:c.6232A>G	XP_005262211.2:p.Asn2078Asp
XM_005262155.3:c.6202A>G	XP_005262212.2:p.Asn2068Asp
XM_005262156.3:c.6154A>G	XP_005262213.2:p.Asn2052Asp
XM_005262157.3:c.6115A>G	XP_005262214.2:p.Asn2039Asp
XM_006724666.2:c.6202A>G	XP_006724729.1:p.Asn2068Asp
XM_006724667.2:c.6040A>G	XP_006724730.1:p.Asn2014Asp
XR_938400.1:n.6661A>G
NM_000489.5:c.6319A>G	NP_000480.3:p.Asn2107Asp
XM_005262153.5:c.6316A>G	XP_005262210.2:p.Asn2106Asp
XM_005262154.5:c.6232A>G	XP_005262211.2:p.Asn2078Asp
XM_005262155.4:c.6202A>G	XP_005262212.2:p.Asn2068Asp
XM_005262156.4:c.6154A>G	XP_005262213.2:p.Asn2052Asp
XM_005262157.5:c.6115A>G	XP_005262214.2:p.Asn2039Asp
XM_006724666.4:c.6202A>G	XP_006724729.1:p.Asn2068Asp
XM_006724667.3:c.6040A>G	XP_006724730.1:p.Asn2014Asp
XM_017029601.2:c.6229A>G	XP_016885090.1:p.Asn2077Asp
XM_017029602.1:c.6199A>G	XP_016885091.1:p.Asn2067Asp
XM_017029603.1:c.6151A>G	XP_016885092.1:p.Asn2051Asp
XM_017029604.2:c.6118A>G	XP_016885093.1:p.Asn2040Asp
XM_017029605.1:c.6115A>G	XP_016885094.1:p.Asn2039Asp
XM_017029606.2:c.6088A>G	XP_016885095.1:p.Asn2030Asp
XM_017029607.2:c.6085A>G	XP_016885096.1:p.Asn2029Asp
XM_017029608.2:c.6037A>G	XP_016885097.1:p.Asn2013Asp
XM_017029609.1:c.6001A>G	XP_016885098.1:p.Asn2001Asp
XM_017029610.1:c.5998A>G	XP_016885099.1:p.Asn2000Asp
XM_017029611.1:c.5953A>G	XP_016885100.1:p.Asn1985Asp
XR_001755700.2:n.6618A>G
NM_138270.4:c.6205A>G	NP_612114.2:p.Asn2069Asp
NM_000489.6:c.6319A>G MANE Select	NP_000480.3:p.Asn2107Asp
NM_138270.5:c.6205A>G	NP_612114.2:p.Asn2069Asp