Canonical Allele Identifier: CA413722494

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76944339T>C (hg19) ; chrX:g.77688846T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77688846T>C , CM000685.2:g.77688846T>C	GRCh38
NC_000023.10:g.76944339T>C , CM000685.1:g.76944339T>C	GRCh37
NC_000023.9:g.76830995T>C	NCBI36
NG_008838.2:g.102376A>G
NG_008838.3:g.102424A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373344.11:c.566A>G MANE Select	ENSP00000362441.4:p.His189Arg
ENST00000373344.9:c.566A>G	ENSP00000362441.4:p.His189Arg
ENST00000395603.7:c.452A>G	ENSP00000378967.3:p.His151Arg
ENST00000480283.5:c.*194A>G	ENSP00000480196.1:n.*194A>G
ENST00000623321.3:c.401A>G	ENSP00000485127.1:p.His134Arg
ENST00000624032.3:c.566A>G	ENSP00000485253.1:p.His189Arg
ENST00000624166.3:c.449A>G	ENSP00000485103.1:p.His150Arg
ENST00000624668.3:c.287A>G	ENSP00000485100.1:p.His96Arg
ENST00000625063.3:c.381A>G
NM_000489.4:c.566A>G	NP_000480.3:p.His189Arg
NM_138270.3:c.452A>G	NP_612114.2:p.His151Arg
XM_005262153.3:c.563A>G	XP_005262210.2:p.His188Arg
XM_005262154.3:c.566A>G	XP_005262211.2:p.His189Arg
XM_005262155.3:c.449A>G	XP_005262212.2:p.His150Arg
XM_005262156.3:c.401A>G	XP_005262213.2:p.His134Arg
XM_005262157.3:c.449A>G	XP_005262214.2:p.His150Arg
XM_006724666.2:c.449A>G	XP_006724729.1:p.His150Arg
XM_006724667.2:c.287A>G	XP_006724730.1:p.His96Arg
XM_006724668.2:c.566A>G	XP_006724731.1:p.His189Arg
XR_938400.1:n.834A>G
NM_000489.5:c.566A>G	NP_000480.3:p.His189Arg
XM_005262153.5:c.563A>G	XP_005262210.2:p.His188Arg
XM_005262154.5:c.566A>G	XP_005262211.2:p.His189Arg
XM_005262155.4:c.449A>G	XP_005262212.2:p.His150Arg
XM_005262156.4:c.401A>G	XP_005262213.2:p.His134Arg
XM_005262157.5:c.449A>G	XP_005262214.2:p.His150Arg
XM_006724666.4:c.449A>G	XP_006724729.1:p.His150Arg
XM_006724667.3:c.287A>G	XP_006724730.1:p.His96Arg
XM_006724668.3:c.566A>G	XP_006724731.1:p.His189Arg
XM_017029601.2:c.563A>G	XP_016885090.1:p.His188Arg
XM_017029602.1:c.446A>G	XP_016885091.1:p.His149Arg
XM_017029603.1:c.398A>G	XP_016885092.1:p.His133Arg
XM_017029604.2:c.452A>G	XP_016885093.1:p.His151Arg
XM_017029605.1:c.449A>G	XP_016885094.1:p.His150Arg
XM_017029606.2:c.335A>G	XP_016885095.1:p.His112Arg
XM_017029607.2:c.332A>G	XP_016885096.1:p.His111Arg
XM_017029608.2:c.284A>G	XP_016885097.1:p.His95Arg
XM_017029609.1:c.335A>G	XP_016885098.1:p.His112Arg
XM_017029610.1:c.332A>G	XP_016885099.1:p.His111Arg
XM_017029611.1:c.287A>G	XP_016885100.1:p.His96Arg
XR_001755700.2:n.791A>G
NM_138270.4:c.452A>G	NP_612114.2:p.His151Arg
NM_000489.6:c.566A>G MANE Select	NP_000480.3:p.His189Arg
NM_138270.5:c.452A>G	NP_612114.2:p.His151Arg