Canonical Allele Identifier: CA413707985

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907665T>C (hg19) ; chrX:g.77652175T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652175T>C , CM000685.2:g.77652175T>C	GRCh38
NC_000023.10:g.76907665T>C , CM000685.1:g.76907665T>C	GRCh37
NC_000023.9:g.76794321T>C	NCBI36
NG_008838.2:g.139047A>G
NG_008838.3:g.139095A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4496A>G MANE Select	ENSP00000362441.4:p.Glu1499Gly
ENST00000373344.9:c.4496A>G	ENSP00000362441.4:p.Glu1499Gly
ENST00000395603.7:c.4382A>G	ENSP00000378967.3:p.Glu1461Gly
ENST00000480283.5:c.*4124A>G	ENSP00000480196.1:n.*4124A>G
ENST00000623242.3:c.102A>G
NM_000489.4:c.4496A>G	NP_000480.3:p.Glu1499Gly
NM_138270.3:c.4382A>G	NP_612114.2:p.Glu1461Gly
XM_005262153.3:c.4493A>G	XP_005262210.2:p.Glu1498Gly
XM_005262154.3:c.4409A>G	XP_005262211.2:p.Glu1470Gly
XM_005262155.3:c.4379A>G	XP_005262212.2:p.Glu1460Gly
XM_005262156.3:c.4331A>G	XP_005262213.2:p.Glu1444Gly
XM_005262157.3:c.4292A>G	XP_005262214.2:p.Glu1431Gly
XM_006724666.2:c.4379A>G	XP_006724729.1:p.Glu1460Gly
XM_006724667.2:c.4217A>G	XP_006724730.1:p.Glu1406Gly
XM_006724668.2:c.4496A>G	XP_006724731.1:p.Glu1499Gly
XR_938400.1:n.4764A>G
NM_000489.5:c.4496A>G	NP_000480.3:p.Glu1499Gly
XM_005262153.5:c.4493A>G	XP_005262210.2:p.Glu1498Gly
XM_005262154.5:c.4409A>G	XP_005262211.2:p.Glu1470Gly
XM_005262155.4:c.4379A>G	XP_005262212.2:p.Glu1460Gly
XM_005262156.4:c.4331A>G	XP_005262213.2:p.Glu1444Gly
XM_005262157.5:c.4292A>G	XP_005262214.2:p.Glu1431Gly
XM_006724666.4:c.4379A>G	XP_006724729.1:p.Glu1460Gly
XM_006724667.3:c.4217A>G	XP_006724730.1:p.Glu1406Gly
XM_006724668.3:c.4496A>G	XP_006724731.1:p.Glu1499Gly
XM_017029601.2:c.4406A>G	XP_016885090.1:p.Glu1469Gly
XM_017029602.1:c.4376A>G	XP_016885091.1:p.Glu1459Gly
XM_017029603.1:c.4328A>G	XP_016885092.1:p.Glu1443Gly
XM_017029604.2:c.4295A>G	XP_016885093.1:p.Glu1432Gly
XM_017029605.1:c.4292A>G	XP_016885094.1:p.Glu1431Gly
XM_017029606.2:c.4265A>G	XP_016885095.1:p.Glu1422Gly
XM_017029607.2:c.4262A>G	XP_016885096.1:p.Glu1421Gly
XM_017029608.2:c.4214A>G	XP_016885097.1:p.Glu1405Gly
XM_017029609.1:c.4178A>G	XP_016885098.1:p.Glu1393Gly
XM_017029610.1:c.4175A>G	XP_016885099.1:p.Glu1392Gly
XM_017029611.1:c.4130A>G	XP_016885100.1:p.Glu1377Gly
XR_001755700.2:n.4721A>G
NM_138270.4:c.4382A>G	NP_612114.2:p.Glu1461Gly
NM_000489.6:c.4496A>G MANE Select	NP_000480.3:p.Glu1499Gly
NM_138270.5:c.4382A>G	NP_612114.2:p.Glu1461Gly