Canonical Allele Identifier: CA413709020

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907840T>C (hg19) ; chrX:g.77652350T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652350T>C , CM000685.2:g.77652350T>C	GRCh38
NC_000023.10:g.76907840T>C , CM000685.1:g.76907840T>C	GRCh37
NC_000023.9:g.76794496T>C	NCBI36
NG_008838.2:g.138872A>G
NG_008838.3:g.138920A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4321A>G MANE Select	ENSP00000362441.4:p.Asn1441Asp
ENST00000373344.9:c.4321A>G	ENSP00000362441.4:p.Asn1441Asp
ENST00000395603.7:c.4207A>G	ENSP00000378967.3:p.Asn1403Asp
ENST00000480283.5:c.*3949A>G	ENSP00000480196.1:n.*3949A>G
NM_000489.4:c.4321A>G	NP_000480.3:p.Asn1441Asp
NM_138270.3:c.4207A>G	NP_612114.2:p.Asn1403Asp
XM_005262153.3:c.4318A>G	XP_005262210.2:p.Asn1440Asp
XM_005262154.3:c.4234A>G	XP_005262211.2:p.Asn1412Asp
XM_005262155.3:c.4204A>G	XP_005262212.2:p.Asn1402Asp
XM_005262156.3:c.4156A>G	XP_005262213.2:p.Asn1386Asp
XM_005262157.3:c.4117A>G	XP_005262214.2:p.Asn1373Asp
XM_006724666.2:c.4204A>G	XP_006724729.1:p.Asn1402Asp
XM_006724667.2:c.4042A>G	XP_006724730.1:p.Asn1348Asp
XM_006724668.2:c.4321A>G	XP_006724731.1:p.Asn1441Asp
XR_938400.1:n.4589A>G
NM_000489.5:c.4321A>G	NP_000480.3:p.Asn1441Asp
XM_005262153.5:c.4318A>G	XP_005262210.2:p.Asn1440Asp
XM_005262154.5:c.4234A>G	XP_005262211.2:p.Asn1412Asp
XM_005262155.4:c.4204A>G	XP_005262212.2:p.Asn1402Asp
XM_005262156.4:c.4156A>G	XP_005262213.2:p.Asn1386Asp
XM_005262157.5:c.4117A>G	XP_005262214.2:p.Asn1373Asp
XM_006724666.4:c.4204A>G	XP_006724729.1:p.Asn1402Asp
XM_006724667.3:c.4042A>G	XP_006724730.1:p.Asn1348Asp
XM_006724668.3:c.4321A>G	XP_006724731.1:p.Asn1441Asp
XM_017029601.2:c.4231A>G	XP_016885090.1:p.Asn1411Asp
XM_017029602.1:c.4201A>G	XP_016885091.1:p.Asn1401Asp
XM_017029603.1:c.4153A>G	XP_016885092.1:p.Asn1385Asp
XM_017029604.2:c.4120A>G	XP_016885093.1:p.Asn1374Asp
XM_017029605.1:c.4117A>G	XP_016885094.1:p.Asn1373Asp
XM_017029606.2:c.4090A>G	XP_016885095.1:p.Asn1364Asp
XM_017029607.2:c.4087A>G	XP_016885096.1:p.Asn1363Asp
XM_017029608.2:c.4039A>G	XP_016885097.1:p.Asn1347Asp
XM_017029609.1:c.4003A>G	XP_016885098.1:p.Asn1335Asp
XM_017029610.1:c.4000A>G	XP_016885099.1:p.Asn1334Asp
XM_017029611.1:c.3955A>G	XP_016885100.1:p.Asn1319Asp
XR_001755700.2:n.4546A>G
NM_138270.4:c.4207A>G	NP_612114.2:p.Asn1403Asp
NM_000489.6:c.4321A>G MANE Select	NP_000480.3:p.Asn1441Asp
NM_138270.5:c.4207A>G	NP_612114.2:p.Asn1403Asp