Canonical Allele Identifier: CA413708660

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907781T>G (hg19) ; chrX:g.77652291T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652291T>G , CM000685.2:g.77652291T>G	GRCh38
NC_000023.10:g.76907781T>G , CM000685.1:g.76907781T>G	GRCh37
NC_000023.9:g.76794437T>G	NCBI36
NG_008838.2:g.138931A>C
NG_008838.3:g.138979A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4380A>C MANE Select	ENSP00000362441.4:p.Glu1460Asp
ENST00000373344.9:c.4380A>C	ENSP00000362441.4:p.Glu1460Asp
ENST00000395603.7:c.4266A>C	ENSP00000378967.3:p.Glu1422Asp
ENST00000480283.5:c.*4008A>C	ENSP00000480196.1:n.*4008A>C
NM_000489.4:c.4380A>C	NP_000480.3:p.Glu1460Asp
NM_138270.3:c.4266A>C	NP_612114.2:p.Glu1422Asp
XM_005262153.3:c.4377A>C	XP_005262210.2:p.Glu1459Asp
XM_005262154.3:c.4293A>C	XP_005262211.2:p.Glu1431Asp
XM_005262155.3:c.4263A>C	XP_005262212.2:p.Glu1421Asp
XM_005262156.3:c.4215A>C	XP_005262213.2:p.Glu1405Asp
XM_005262157.3:c.4176A>C	XP_005262214.2:p.Glu1392Asp
XM_006724666.2:c.4263A>C	XP_006724729.1:p.Glu1421Asp
XM_006724667.2:c.4101A>C	XP_006724730.1:p.Glu1367Asp
XM_006724668.2:c.4380A>C	XP_006724731.1:p.Glu1460Asp
XR_938400.1:n.4648A>C
NM_000489.5:c.4380A>C	NP_000480.3:p.Glu1460Asp
XM_005262153.5:c.4377A>C	XP_005262210.2:p.Glu1459Asp
XM_005262154.5:c.4293A>C	XP_005262211.2:p.Glu1431Asp
XM_005262155.4:c.4263A>C	XP_005262212.2:p.Glu1421Asp
XM_005262156.4:c.4215A>C	XP_005262213.2:p.Glu1405Asp
XM_005262157.5:c.4176A>C	XP_005262214.2:p.Glu1392Asp
XM_006724666.4:c.4263A>C	XP_006724729.1:p.Glu1421Asp
XM_006724667.3:c.4101A>C	XP_006724730.1:p.Glu1367Asp
XM_006724668.3:c.4380A>C	XP_006724731.1:p.Glu1460Asp
XM_017029601.2:c.4290A>C	XP_016885090.1:p.Glu1430Asp
XM_017029602.1:c.4260A>C	XP_016885091.1:p.Glu1420Asp
XM_017029603.1:c.4212A>C	XP_016885092.1:p.Glu1404Asp
XM_017029604.2:c.4179A>C	XP_016885093.1:p.Glu1393Asp
XM_017029605.1:c.4176A>C	XP_016885094.1:p.Glu1392Asp
XM_017029606.2:c.4149A>C	XP_016885095.1:p.Glu1383Asp
XM_017029607.2:c.4146A>C	XP_016885096.1:p.Glu1382Asp
XM_017029608.2:c.4098A>C	XP_016885097.1:p.Glu1366Asp
XM_017029609.1:c.4062A>C	XP_016885098.1:p.Glu1354Asp
XM_017029610.1:c.4059A>C	XP_016885099.1:p.Glu1353Asp
XM_017029611.1:c.4014A>C	XP_016885100.1:p.Glu1338Asp
XR_001755700.2:n.4605A>C
NM_138270.4:c.4266A>C	NP_612114.2:p.Glu1422Asp
NM_000489.6:c.4380A>C MANE Select	NP_000480.3:p.Glu1460Asp
NM_138270.5:c.4266A>C	NP_612114.2:p.Glu1422Asp