Canonical Allele Identifier: CA413704905

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76764044G>A (hg19) ; chrX:g.77508566G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508566G>A , CM000685.2:g.77508566G>A	GRCh38
NC_000023.10:g.76764044G>A , CM000685.1:g.76764044G>A	GRCh37
NC_000023.9:g.76650700G>A	NCBI36
NG_008838.2:g.282656C>T
NG_008838.3:g.282704C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7264C>T MANE Select	ENSP00000362441.4:p.Gln2422Ter
ENST00000675732.1:c.2362C>T	ENSP00000502598.1:p.Gln788Ter
ENST00000373344.9:c.7264C>T	ENSP00000362441.4:p.Gln2422Ter
ENST00000395603.7:c.7150C>T	ENSP00000378967.3:p.Gln2384Ter
ENST00000480283.5:c.*6892C>T	ENSP00000480196.1:n.*6892C>T
ENST00000623706.3:n.5584C>T
ENST00000624766.1:n.495C>T
NM_000489.4:c.7264C>T	NP_000480.3:p.Gln2422Ter
NM_138270.3:c.7150C>T	NP_612114.2:p.Gln2384Ter
XM_005262153.3:c.7261C>T	XP_005262210.2:p.Gln2421Ter
XM_005262154.3:c.7177C>T	XP_005262211.2:p.Gln2393Ter
XM_005262155.3:c.7147C>T	XP_005262212.2:p.Gln2383Ter
XM_005262156.3:c.7099C>T	XP_005262213.2:p.Gln2367Ter
XM_005262157.3:c.7060C>T	XP_005262214.2:p.Gln2354Ter
XM_006724666.2:c.7147C>T	XP_006724729.1:p.Gln2383Ter
XM_006724667.2:c.6985C>T	XP_006724730.1:p.Gln2329Ter
XR_938400.1:n.8856C>T
NM_000489.5:c.7264C>T	NP_000480.3:p.Gln2422Ter
XM_005262153.5:c.7261C>T	XP_005262210.2:p.Gln2421Ter
XM_005262154.5:c.7177C>T	XP_005262211.2:p.Gln2393Ter
XM_005262155.4:c.7147C>T	XP_005262212.2:p.Gln2383Ter
XM_005262156.4:c.7099C>T	XP_005262213.2:p.Gln2367Ter
XM_005262157.5:c.7060C>T	XP_005262214.2:p.Gln2354Ter
XM_006724666.4:c.7147C>T	XP_006724729.1:p.Gln2383Ter
XM_006724667.3:c.6985C>T	XP_006724730.1:p.Gln2329Ter
XM_017029601.2:c.7174C>T	XP_016885090.1:p.Gln2392Ter
XM_017029602.1:c.7144C>T	XP_016885091.1:p.Gln2382Ter
XM_017029603.1:c.7096C>T	XP_016885092.1:p.Gln2366Ter
XM_017029604.2:c.7063C>T	XP_016885093.1:p.Gln2355Ter
XM_017029605.1:c.7060C>T	XP_016885094.1:p.Gln2354Ter
XM_017029606.2:c.7033C>T	XP_016885095.1:p.Gln2345Ter
XM_017029607.2:c.7030C>T	XP_016885096.1:p.Gln2344Ter
XM_017029608.2:c.6982C>T	XP_016885097.1:p.Gln2328Ter
XM_017029609.1:c.6946C>T	XP_016885098.1:p.Gln2316Ter
XM_017029610.1:c.6943C>T	XP_016885099.1:p.Gln2315Ter
XM_017029611.1:c.6898C>T	XP_016885100.1:p.Gln2300Ter
XR_001755700.2:n.7563C>T
NM_138270.4:c.7150C>T	NP_612114.2:p.Gln2384Ter
NM_000489.6:c.7264C>T MANE Select	NP_000480.3:p.Gln2422Ter
NM_138270.5:c.7150C>T	NP_612114.2:p.Gln2384Ter