Canonical Allele Identifier: CA413709015

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907839T>G (hg19) ; chrX:g.77652349T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652349T>G , CM000685.2:g.77652349T>G	GRCh38
NC_000023.10:g.76907839T>G , CM000685.1:g.76907839T>G	GRCh37
NC_000023.9:g.76794495T>G	NCBI36
NG_008838.2:g.138873A>C
NG_008838.3:g.138921A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4322A>C MANE Select	ENSP00000362441.4:p.Asn1441Thr
ENST00000373344.9:c.4322A>C	ENSP00000362441.4:p.Asn1441Thr
ENST00000395603.7:c.4208A>C	ENSP00000378967.3:p.Asn1403Thr
ENST00000480283.5:c.*3950A>C	ENSP00000480196.1:n.*3950A>C
NM_000489.4:c.4322A>C	NP_000480.3:p.Asn1441Thr
NM_138270.3:c.4208A>C	NP_612114.2:p.Asn1403Thr
XM_005262153.3:c.4319A>C	XP_005262210.2:p.Asn1440Thr
XM_005262154.3:c.4235A>C	XP_005262211.2:p.Asn1412Thr
XM_005262155.3:c.4205A>C	XP_005262212.2:p.Asn1402Thr
XM_005262156.3:c.4157A>C	XP_005262213.2:p.Asn1386Thr
XM_005262157.3:c.4118A>C	XP_005262214.2:p.Asn1373Thr
XM_006724666.2:c.4205A>C	XP_006724729.1:p.Asn1402Thr
XM_006724667.2:c.4043A>C	XP_006724730.1:p.Asn1348Thr
XM_006724668.2:c.4322A>C	XP_006724731.1:p.Asn1441Thr
XR_938400.1:n.4590A>C
NM_000489.5:c.4322A>C	NP_000480.3:p.Asn1441Thr
XM_005262153.5:c.4319A>C	XP_005262210.2:p.Asn1440Thr
XM_005262154.5:c.4235A>C	XP_005262211.2:p.Asn1412Thr
XM_005262155.4:c.4205A>C	XP_005262212.2:p.Asn1402Thr
XM_005262156.4:c.4157A>C	XP_005262213.2:p.Asn1386Thr
XM_005262157.5:c.4118A>C	XP_005262214.2:p.Asn1373Thr
XM_006724666.4:c.4205A>C	XP_006724729.1:p.Asn1402Thr
XM_006724667.3:c.4043A>C	XP_006724730.1:p.Asn1348Thr
XM_006724668.3:c.4322A>C	XP_006724731.1:p.Asn1441Thr
XM_017029601.2:c.4232A>C	XP_016885090.1:p.Asn1411Thr
XM_017029602.1:c.4202A>C	XP_016885091.1:p.Asn1401Thr
XM_017029603.1:c.4154A>C	XP_016885092.1:p.Asn1385Thr
XM_017029604.2:c.4121A>C	XP_016885093.1:p.Asn1374Thr
XM_017029605.1:c.4118A>C	XP_016885094.1:p.Asn1373Thr
XM_017029606.2:c.4091A>C	XP_016885095.1:p.Asn1364Thr
XM_017029607.2:c.4088A>C	XP_016885096.1:p.Asn1363Thr
XM_017029608.2:c.4040A>C	XP_016885097.1:p.Asn1347Thr
XM_017029609.1:c.4004A>C	XP_016885098.1:p.Asn1335Thr
XM_017029610.1:c.4001A>C	XP_016885099.1:p.Asn1334Thr
XM_017029611.1:c.3956A>C	XP_016885100.1:p.Asn1319Thr
XR_001755700.2:n.4547A>C
NM_138270.4:c.4208A>C	NP_612114.2:p.Asn1403Thr
NM_000489.6:c.4322A>C MANE Select	NP_000480.3:p.Asn1441Thr
NM_138270.5:c.4208A>C	NP_612114.2:p.Asn1403Thr