Canonical Allele Identifier: CA413708265

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907716T>G (hg19) ; chrX:g.77652226T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652226T>G , CM000685.2:g.77652226T>G	GRCh38
NC_000023.10:g.76907716T>G , CM000685.1:g.76907716T>G	GRCh37
NC_000023.9:g.76794372T>G	NCBI36
NG_008838.2:g.138996A>C
NG_008838.3:g.139044A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4445A>C MANE Select	ENSP00000362441.4:p.Lys1482Thr
ENST00000373344.9:c.4445A>C	ENSP00000362441.4:p.Lys1482Thr
ENST00000395603.7:c.4331A>C	ENSP00000378967.3:p.Lys1444Thr
ENST00000480283.5:c.*4073A>C	ENSP00000480196.1:n.*4073A>C
ENST00000623242.3:c.51A>C
NM_000489.4:c.4445A>C	NP_000480.3:p.Lys1482Thr
NM_138270.3:c.4331A>C	NP_612114.2:p.Lys1444Thr
XM_005262153.3:c.4442A>C	XP_005262210.2:p.Lys1481Thr
XM_005262154.3:c.4358A>C	XP_005262211.2:p.Lys1453Thr
XM_005262155.3:c.4328A>C	XP_005262212.2:p.Lys1443Thr
XM_005262156.3:c.4280A>C	XP_005262213.2:p.Lys1427Thr
XM_005262157.3:c.4241A>C	XP_005262214.2:p.Lys1414Thr
XM_006724666.2:c.4328A>C	XP_006724729.1:p.Lys1443Thr
XM_006724667.2:c.4166A>C	XP_006724730.1:p.Lys1389Thr
XM_006724668.2:c.4445A>C	XP_006724731.1:p.Lys1482Thr
XR_938400.1:n.4713A>C
NM_000489.5:c.4445A>C	NP_000480.3:p.Lys1482Thr
XM_005262153.5:c.4442A>C	XP_005262210.2:p.Lys1481Thr
XM_005262154.5:c.4358A>C	XP_005262211.2:p.Lys1453Thr
XM_005262155.4:c.4328A>C	XP_005262212.2:p.Lys1443Thr
XM_005262156.4:c.4280A>C	XP_005262213.2:p.Lys1427Thr
XM_005262157.5:c.4241A>C	XP_005262214.2:p.Lys1414Thr
XM_006724666.4:c.4328A>C	XP_006724729.1:p.Lys1443Thr
XM_006724667.3:c.4166A>C	XP_006724730.1:p.Lys1389Thr
XM_006724668.3:c.4445A>C	XP_006724731.1:p.Lys1482Thr
XM_017029601.2:c.4355A>C	XP_016885090.1:p.Lys1452Thr
XM_017029602.1:c.4325A>C	XP_016885091.1:p.Lys1442Thr
XM_017029603.1:c.4277A>C	XP_016885092.1:p.Lys1426Thr
XM_017029604.2:c.4244A>C	XP_016885093.1:p.Lys1415Thr
XM_017029605.1:c.4241A>C	XP_016885094.1:p.Lys1414Thr
XM_017029606.2:c.4214A>C	XP_016885095.1:p.Lys1405Thr
XM_017029607.2:c.4211A>C	XP_016885096.1:p.Lys1404Thr
XM_017029608.2:c.4163A>C	XP_016885097.1:p.Lys1388Thr
XM_017029609.1:c.4127A>C	XP_016885098.1:p.Lys1376Thr
XM_017029610.1:c.4124A>C	XP_016885099.1:p.Lys1375Thr
XM_017029611.1:c.4079A>C	XP_016885100.1:p.Lys1360Thr
XR_001755700.2:n.4670A>C
NM_138270.4:c.4331A>C	NP_612114.2:p.Lys1444Thr
NM_000489.6:c.4445A>C MANE Select	NP_000480.3:p.Lys1482Thr
NM_138270.5:c.4331A>C	NP_612114.2:p.Lys1444Thr