Canonical Allele Identifier: CA413722516

Gene: ATRX

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000373344.11:c.557T>G MANE Select	ENSP00000362441.4:p.Ile186Ser
ENST00000373344.9:c.557T>G	ENSP00000362441.4:p.Ile186Ser
ENST00000395603.7:c.443T>G	ENSP00000378967.3:p.Ile148Ser
ENST00000480283.5:c.*185T>G	ENSP00000480196.1:n.*185T>G
ENST00000623321.3:c.392T>G	ENSP00000485127.1:p.Ile131Ser
ENST00000624032.3:c.557T>G	ENSP00000485253.1:p.Ile186Ser
ENST00000624166.3:c.440T>G	ENSP00000485103.1:p.Ile147Ser
ENST00000624668.3:c.278T>G	ENSP00000485100.1:p.Ile93Ser
ENST00000625063.3:c.372T>G
NM_000489.4:c.557T>G	NP_000480.3:p.Ile186Ser
NM_138270.3:c.443T>G	NP_612114.2:p.Ile148Ser
XM_005262153.3:c.554T>G	XP_005262210.2:p.Ile185Ser
XM_005262154.3:c.557T>G	XP_005262211.2:p.Ile186Ser
XM_005262155.3:c.440T>G	XP_005262212.2:p.Ile147Ser
XM_005262156.3:c.392T>G	XP_005262213.2:p.Ile131Ser
XM_005262157.3:c.440T>G	XP_005262214.2:p.Ile147Ser
XM_006724666.2:c.440T>G	XP_006724729.1:p.Ile147Ser
XM_006724667.2:c.278T>G	XP_006724730.1:p.Ile93Ser
XM_006724668.2:c.557T>G	XP_006724731.1:p.Ile186Ser
XR_938400.1:n.825T>G
NM_000489.5:c.557T>G	NP_000480.3:p.Ile186Ser
XM_005262153.5:c.554T>G	XP_005262210.2:p.Ile185Ser
XM_005262154.5:c.557T>G	XP_005262211.2:p.Ile186Ser
XM_005262155.4:c.440T>G	XP_005262212.2:p.Ile147Ser
XM_005262156.4:c.392T>G	XP_005262213.2:p.Ile131Ser
XM_005262157.5:c.440T>G	XP_005262214.2:p.Ile147Ser
XM_006724666.4:c.440T>G	XP_006724729.1:p.Ile147Ser
XM_006724667.3:c.278T>G	XP_006724730.1:p.Ile93Ser
XM_006724668.3:c.557T>G	XP_006724731.1:p.Ile186Ser
XM_017029601.2:c.554T>G	XP_016885090.1:p.Ile185Ser
XM_017029602.1:c.437T>G	XP_016885091.1:p.Ile146Ser
XM_017029603.1:c.389T>G	XP_016885092.1:p.Ile130Ser
XM_017029604.2:c.443T>G	XP_016885093.1:p.Ile148Ser
XM_017029605.1:c.440T>G	XP_016885094.1:p.Ile147Ser
XM_017029606.2:c.326T>G	XP_016885095.1:p.Ile109Ser
XM_017029607.2:c.323T>G	XP_016885096.1:p.Ile108Ser
XM_017029608.2:c.275T>G	XP_016885097.1:p.Ile92Ser
XM_017029609.1:c.326T>G	XP_016885098.1:p.Ile109Ser
XM_017029610.1:c.323T>G	XP_016885099.1:p.Ile108Ser
XM_017029611.1:c.278T>G	XP_016885100.1:p.Ile93Ser
XR_001755700.2:n.782T>G
NM_138270.4:c.443T>G	NP_612114.2:p.Ile148Ser
NM_000489.6:c.557T>G MANE Select	NP_000480.3:p.Ile186Ser
NM_138270.5:c.443T>G	NP_612114.2:p.Ile148Ser