Canonical Allele Identifier: CA413722518

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76944348A>T (hg19) ; chrX:g.77688855A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77688855A>T , CM000685.2:g.77688855A>T	GRCh38
NC_000023.10:g.76944348A>T , CM000685.1:g.76944348A>T	GRCh37
NC_000023.9:g.76831004A>T	NCBI36
NG_008838.2:g.102367T>A
NG_008838.3:g.102415T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373344.11:c.557T>A MANE Select	ENSP00000362441.4:p.Ile186Asn
ENST00000373344.9:c.557T>A	ENSP00000362441.4:p.Ile186Asn
ENST00000395603.7:c.443T>A	ENSP00000378967.3:p.Ile148Asn
ENST00000480283.5:c.*185T>A	ENSP00000480196.1:n.*185T>A
ENST00000623321.3:c.392T>A	ENSP00000485127.1:p.Ile131Asn
ENST00000624032.3:c.557T>A	ENSP00000485253.1:p.Ile186Asn
ENST00000624166.3:c.440T>A	ENSP00000485103.1:p.Ile147Asn
ENST00000624668.3:c.278T>A	ENSP00000485100.1:p.Ile93Asn
ENST00000625063.3:c.372T>A
NM_000489.4:c.557T>A	NP_000480.3:p.Ile186Asn
NM_138270.3:c.443T>A	NP_612114.2:p.Ile148Asn
XM_005262153.3:c.554T>A	XP_005262210.2:p.Ile185Asn
XM_005262154.3:c.557T>A	XP_005262211.2:p.Ile186Asn
XM_005262155.3:c.440T>A	XP_005262212.2:p.Ile147Asn
XM_005262156.3:c.392T>A	XP_005262213.2:p.Ile131Asn
XM_005262157.3:c.440T>A	XP_005262214.2:p.Ile147Asn
XM_006724666.2:c.440T>A	XP_006724729.1:p.Ile147Asn
XM_006724667.2:c.278T>A	XP_006724730.1:p.Ile93Asn
XM_006724668.2:c.557T>A	XP_006724731.1:p.Ile186Asn
XR_938400.1:n.825T>A
NM_000489.5:c.557T>A	NP_000480.3:p.Ile186Asn
XM_005262153.5:c.554T>A	XP_005262210.2:p.Ile185Asn
XM_005262154.5:c.557T>A	XP_005262211.2:p.Ile186Asn
XM_005262155.4:c.440T>A	XP_005262212.2:p.Ile147Asn
XM_005262156.4:c.392T>A	XP_005262213.2:p.Ile131Asn
XM_005262157.5:c.440T>A	XP_005262214.2:p.Ile147Asn
XM_006724666.4:c.440T>A	XP_006724729.1:p.Ile147Asn
XM_006724667.3:c.278T>A	XP_006724730.1:p.Ile93Asn
XM_006724668.3:c.557T>A	XP_006724731.1:p.Ile186Asn
XM_017029601.2:c.554T>A	XP_016885090.1:p.Ile185Asn
XM_017029602.1:c.437T>A	XP_016885091.1:p.Ile146Asn
XM_017029603.1:c.389T>A	XP_016885092.1:p.Ile130Asn
XM_017029604.2:c.443T>A	XP_016885093.1:p.Ile148Asn
XM_017029605.1:c.440T>A	XP_016885094.1:p.Ile147Asn
XM_017029606.2:c.326T>A	XP_016885095.1:p.Ile109Asn
XM_017029607.2:c.323T>A	XP_016885096.1:p.Ile108Asn
XM_017029608.2:c.275T>A	XP_016885097.1:p.Ile92Asn
XM_017029609.1:c.326T>A	XP_016885098.1:p.Ile109Asn
XM_017029610.1:c.323T>A	XP_016885099.1:p.Ile108Asn
XM_017029611.1:c.278T>A	XP_016885100.1:p.Ile93Asn
XR_001755700.2:n.782T>A
NM_138270.4:c.443T>A	NP_612114.2:p.Ile148Asn
NM_000489.6:c.557T>A MANE Select	NP_000480.3:p.Ile186Asn
NM_138270.5:c.443T>A	NP_612114.2:p.Ile148Asn