Canonical Allele Identifier: CA413707325

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76937537C>G (hg19) ; chrX:g.77682045C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77682045C>G , CM000685.2:g.77682045C>G	GRCh38
NC_000023.10:g.76937537C>G , CM000685.1:g.76937537C>G	GRCh37
NC_000023.9:g.76824193C>G	NCBI36
NG_008838.2:g.109177G>C
NG_008838.3:g.109225G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.3211G>C MANE Select	ENSP00000362441.4:p.Gly1071Arg
ENST00000373344.9:c.3211G>C	ENSP00000362441.4:p.Gly1071Arg
ENST00000395603.7:c.3097G>C	ENSP00000378967.3:p.Gly1033Arg
ENST00000480283.5:c.*2839G>C	ENSP00000480196.1:n.*2839G>C
ENST00000493470.2:c.97G>C	ENSP00000485408.1:p.Gly33Arg
ENST00000624166.3:c.3007G>C	ENSP00000485103.1:p.Gly1003Arg
NM_000489.4:c.3211G>C	NP_000480.3:p.Gly1071Arg
NM_138270.3:c.3097G>C	NP_612114.2:p.Gly1033Arg
XM_005262153.3:c.3208G>C	XP_005262210.2:p.Gly1070Arg
XM_005262154.3:c.3124G>C	XP_005262211.2:p.Gly1042Arg
XM_005262155.3:c.3094G>C	XP_005262212.2:p.Gly1032Arg
XM_005262156.3:c.3046G>C	XP_005262213.2:p.Gly1016Arg
XM_005262157.3:c.3007G>C	XP_005262214.2:p.Gly1003Arg
XM_006724666.2:c.3094G>C	XP_006724729.1:p.Gly1032Arg
XM_006724667.2:c.2932G>C	XP_006724730.1:p.Gly978Arg
XM_006724668.2:c.3211G>C	XP_006724731.1:p.Gly1071Arg
XR_938400.1:n.3479G>C
NM_000489.5:c.3211G>C	NP_000480.3:p.Gly1071Arg
XM_005262153.5:c.3208G>C	XP_005262210.2:p.Gly1070Arg
XM_005262154.5:c.3124G>C	XP_005262211.2:p.Gly1042Arg
XM_005262155.4:c.3094G>C	XP_005262212.2:p.Gly1032Arg
XM_005262156.4:c.3046G>C	XP_005262213.2:p.Gly1016Arg
XM_005262157.5:c.3007G>C	XP_005262214.2:p.Gly1003Arg
XM_006724666.4:c.3094G>C	XP_006724729.1:p.Gly1032Arg
XM_006724667.3:c.2932G>C	XP_006724730.1:p.Gly978Arg
XM_006724668.3:c.3211G>C	XP_006724731.1:p.Gly1071Arg
XM_017029601.2:c.3121G>C	XP_016885090.1:p.Gly1041Arg
XM_017029602.1:c.3091G>C	XP_016885091.1:p.Gly1031Arg
XM_017029603.1:c.3043G>C	XP_016885092.1:p.Gly1015Arg
XM_017029604.2:c.3010G>C	XP_016885093.1:p.Gly1004Arg
XM_017029605.1:c.3007G>C	XP_016885094.1:p.Gly1003Arg
XM_017029606.2:c.2980G>C	XP_016885095.1:p.Gly994Arg
XM_017029607.2:c.2977G>C	XP_016885096.1:p.Gly993Arg
XM_017029608.2:c.2929G>C	XP_016885097.1:p.Gly977Arg
XM_017029609.1:c.2893G>C	XP_016885098.1:p.Gly965Arg
XM_017029610.1:c.2890G>C	XP_016885099.1:p.Gly964Arg
XM_017029611.1:c.2845G>C	XP_016885100.1:p.Gly949Arg
XR_001755700.2:n.3436G>C
NM_138270.4:c.3097G>C	NP_612114.2:p.Gly1033Arg
NM_000489.6:c.3211G>C MANE Select	NP_000480.3:p.Gly1071Arg
NM_138270.5:c.3097G>C	NP_612114.2:p.Gly1033Arg