Canonical Allele Identifier: CA413704928

Gene: ATRX

Linked Data

• dbSNP Id: rs2147651671
• MyVariant Identifiers: chrX:g.76764047G>C (hg19) ; chrX:g.77508569G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508569G>C , CM000685.2:g.77508569G>C	GRCh38
NC_000023.10:g.76764047G>C , CM000685.1:g.76764047G>C	GRCh37
NC_000023.9:g.76650703G>C	NCBI36
NG_008838.2:g.282653C>G
NG_008838.3:g.282701C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7261C>G MANE Select	ENSP00000362441.4:p.Gln2421Glu
ENST00000675732.1:c.2359C>G	ENSP00000502598.1:p.Gln787Glu
ENST00000373344.9:c.7261C>G	ENSP00000362441.4:p.Gln2421Glu
ENST00000395603.7:c.7147C>G	ENSP00000378967.3:p.Gln2383Glu
ENST00000480283.5:c.*6889C>G	ENSP00000480196.1:n.*6889C>G
ENST00000623706.3:n.5581C>G
ENST00000624766.1:n.492C>G
NM_000489.4:c.7261C>G	NP_000480.3:p.Gln2421Glu
NM_138270.3:c.7147C>G	NP_612114.2:p.Gln2383Glu
XM_005262153.3:c.7258C>G	XP_005262210.2:p.Gln2420Glu
XM_005262154.3:c.7174C>G	XP_005262211.2:p.Gln2392Glu
XM_005262155.3:c.7144C>G	XP_005262212.2:p.Gln2382Glu
XM_005262156.3:c.7096C>G	XP_005262213.2:p.Gln2366Glu
XM_005262157.3:c.7057C>G	XP_005262214.2:p.Gln2353Glu
XM_006724666.2:c.7144C>G	XP_006724729.1:p.Gln2382Glu
XM_006724667.2:c.6982C>G	XP_006724730.1:p.Gln2328Glu
XR_938400.1:n.8853C>G
NM_000489.5:c.7261C>G	NP_000480.3:p.Gln2421Glu
XM_005262153.5:c.7258C>G	XP_005262210.2:p.Gln2420Glu
XM_005262154.5:c.7174C>G	XP_005262211.2:p.Gln2392Glu
XM_005262155.4:c.7144C>G	XP_005262212.2:p.Gln2382Glu
XM_005262156.4:c.7096C>G	XP_005262213.2:p.Gln2366Glu
XM_005262157.5:c.7057C>G	XP_005262214.2:p.Gln2353Glu
XM_006724666.4:c.7144C>G	XP_006724729.1:p.Gln2382Glu
XM_006724667.3:c.6982C>G	XP_006724730.1:p.Gln2328Glu
XM_017029601.2:c.7171C>G	XP_016885090.1:p.Gln2391Glu
XM_017029602.1:c.7141C>G	XP_016885091.1:p.Gln2381Glu
XM_017029603.1:c.7093C>G	XP_016885092.1:p.Gln2365Glu
XM_017029604.2:c.7060C>G	XP_016885093.1:p.Gln2354Glu
XM_017029605.1:c.7057C>G	XP_016885094.1:p.Gln2353Glu
XM_017029606.2:c.7030C>G	XP_016885095.1:p.Gln2344Glu
XM_017029607.2:c.7027C>G	XP_016885096.1:p.Gln2343Glu
XM_017029608.2:c.6979C>G	XP_016885097.1:p.Gln2327Glu
XM_017029609.1:c.6943C>G	XP_016885098.1:p.Gln2315Glu
XM_017029610.1:c.6940C>G	XP_016885099.1:p.Gln2314Glu
XM_017029611.1:c.6895C>G	XP_016885100.1:p.Gln2299Glu
XR_001755700.2:n.7560C>G
NM_138270.4:c.7147C>G	NP_612114.2:p.Gln2383Glu
NM_000489.6:c.7261C>G MANE Select	NP_000480.3:p.Gln2421Glu
NM_138270.5:c.7147C>G	NP_612114.2:p.Gln2383Glu