Canonical Allele Identifier: CA413718892

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77684003C>T , CM000685.2:g.77684003C>T	GRCh38
NC_000023.10:g.76939495C>T , CM000685.1:g.76939495C>T	GRCh37
NC_000023.9:g.76826151C>T	NCBI36
NG_008838.2:g.107219G>A
NG_008838.3:g.107267G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000489.6:c.1253G>A MANE Select	NP_000480.3:p.Arg418Gln
ENST00000373344.11:c.1253G>A MANE Select	ENSP00000362441.4:p.Arg418Gln
NM_000489.4:c.1253G>A	NP_000480.3:p.Arg418Gln
NM_000489.5:c.1253G>A	NP_000480.3:p.Arg418Gln
NM_138270.3:c.1139G>A	NP_612114.2:p.Arg380Gln
NM_138270.4:c.1139G>A	NP_612114.2:p.Arg380Gln
NM_138270.5:c.1139G>A	NP_612114.2:p.Arg380Gln
ENST00000373344.9:c.1253G>A	ENSP00000362441.4:p.Arg418Gln
ENST00000395603.7:c.1139G>A	ENSP00000378967.3:p.Arg380Gln
ENST00000480283.5:c.*881G>A	ENSP00000480196.1:n.*881G>A
ENST00000623321.3:c.1088G>A	ENSP00000485127.1:p.Arg363Gln
ENST00000624032.3:c.1253G>A	ENSP00000485253.1:p.Arg418Gln
ENST00000624166.3:c.1136G>A	ENSP00000485103.1:p.Arg379Gln
XM_005262153.3:c.1250G>A	XP_005262210.2:p.Arg417Gln
XM_005262153.5:c.1250G>A	XP_005262210.2:p.Arg417Gln
XM_005262154.3:c.1253G>A	XP_005262211.2:p.Arg418Gln
XM_005262154.5:c.1253G>A	XP_005262211.2:p.Arg418Gln
XM_005262155.3:c.1136G>A	XP_005262212.2:p.Arg379Gln
XM_005262155.4:c.1136G>A	XP_005262212.2:p.Arg379Gln
XM_005262156.3:c.1088G>A	XP_005262213.2:p.Arg363Gln
XM_005262156.4:c.1088G>A	XP_005262213.2:p.Arg363Gln
XM_005262157.3:c.1136G>A	XP_005262214.2:p.Arg379Gln
XM_005262157.5:c.1136G>A	XP_005262214.2:p.Arg379Gln
XM_006724666.2:c.1136G>A	XP_006724729.1:p.Arg379Gln
XM_006724666.4:c.1136G>A	XP_006724729.1:p.Arg379Gln
XM_006724667.2:c.974G>A	XP_006724730.1:p.Arg325Gln
XM_006724667.3:c.974G>A	XP_006724730.1:p.Arg325Gln
XM_006724668.2:c.1253G>A	XP_006724731.1:p.Arg418Gln
XM_006724668.3:c.1253G>A	XP_006724731.1:p.Arg418Gln
XM_017029601.2:c.1250G>A	XP_016885090.1:p.Arg417Gln
XM_017029602.1:c.1133G>A	XP_016885091.1:p.Arg378Gln
XM_017029603.1:c.1085G>A	XP_016885092.1:p.Arg362Gln
XM_017029604.2:c.1139G>A	XP_016885093.1:p.Arg380Gln
XM_017029605.1:c.1136G>A	XP_016885094.1:p.Arg379Gln
XM_017029606.2:c.1022G>A	XP_016885095.1:p.Arg341Gln
XM_017029607.2:c.1019G>A	XP_016885096.1:p.Arg340Gln
XM_017029608.2:c.971G>A	XP_016885097.1:p.Arg324Gln
XM_017029609.1:c.1022G>A	XP_016885098.1:p.Arg341Gln
XM_017029610.1:c.1019G>A	XP_016885099.1:p.Arg340Gln
XM_017029611.1:c.974G>A	XP_016885100.1:p.Arg325Gln
XR_001755700.2:n.1478G>A
XR_938400.1:n.1521G>A