Canonical Allele Identifier: CA517471472

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907730T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652240T>C , CM000685.2:g.77652240T>C	GRCh38
NC_000023.10:g.76907730T>C , CM000685.1:g.76907730T>C	GRCh37
NC_000023.9:g.76794386T>C	NCBI36
NG_008838.2:g.138982A>G
NG_008838.3:g.139030A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4431A>G MANE Select	ENSP00000362441.4:p.Arg1477=
ENST00000373344.9:c.4431A>G	ENSP00000362441.4:p.Arg1477=
ENST00000395603.7:c.4317A>G	ENSP00000378967.3:p.Arg1439=
ENST00000480283.5:c.*4059A>G	ENSP00000480196.1:n.*4059A>G
ENST00000623242.3:c.37A>G
NM_000489.4:c.4431A>G	NP_000480.3:p.Arg1477=
NM_138270.3:c.4317A>G	NP_612114.2:p.Arg1439=
XM_005262153.3:c.4428A>G	XP_005262210.2:p.Arg1476=
XM_005262154.3:c.4344A>G	XP_005262211.2:p.Arg1448=
XM_005262155.3:c.4314A>G	XP_005262212.2:p.Arg1438=
XM_005262156.3:c.4266A>G	XP_005262213.2:p.Arg1422=
XM_005262157.3:c.4227A>G	XP_005262214.2:p.Arg1409=
XM_006724666.2:c.4314A>G	XP_006724729.1:p.Arg1438=
XM_006724667.2:c.4152A>G	XP_006724730.1:p.Arg1384=
XM_006724668.2:c.4431A>G	XP_006724731.1:p.Arg1477=
XR_938400.1:n.4699A>G
NM_000489.5:c.4431A>G	NP_000480.3:p.Arg1477=
XM_005262153.5:c.4428A>G	XP_005262210.2:p.Arg1476=
XM_005262154.5:c.4344A>G	XP_005262211.2:p.Arg1448=
XM_005262155.4:c.4314A>G	XP_005262212.2:p.Arg1438=
XM_005262156.4:c.4266A>G	XP_005262213.2:p.Arg1422=
XM_005262157.5:c.4227A>G	XP_005262214.2:p.Arg1409=
XM_006724666.4:c.4314A>G	XP_006724729.1:p.Arg1438=
XM_006724667.3:c.4152A>G	XP_006724730.1:p.Arg1384=
XM_006724668.3:c.4431A>G	XP_006724731.1:p.Arg1477=
XM_017029601.2:c.4341A>G	XP_016885090.1:p.Arg1447=
XM_017029602.1:c.4311A>G	XP_016885091.1:p.Arg1437=
XM_017029603.1:c.4263A>G	XP_016885092.1:p.Arg1421=
XM_017029604.2:c.4230A>G	XP_016885093.1:p.Arg1410=
XM_017029605.1:c.4227A>G	XP_016885094.1:p.Arg1409=
XM_017029606.2:c.4200A>G	XP_016885095.1:p.Arg1400=
XM_017029607.2:c.4197A>G	XP_016885096.1:p.Arg1399=
XM_017029608.2:c.4149A>G	XP_016885097.1:p.Arg1383=
XM_017029609.1:c.4113A>G	XP_016885098.1:p.Arg1371=
XM_017029610.1:c.4110A>G	XP_016885099.1:p.Arg1370=
XM_017029611.1:c.4065A>G	XP_016885100.1:p.Arg1355=
XR_001755700.2:n.4656A>G
NM_138270.4:c.4317A>G	NP_612114.2:p.Arg1439=
NM_000489.6:c.4431A>G MANE Select	NP_000480.3:p.Arg1477=
NM_138270.5:c.4317A>G	NP_612114.2:p.Arg1439=