Canonical Allele Identifier: CA413703710

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763884G>C (hg19) ; chrX:g.77508406G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508406G>C , CM000685.2:g.77508406G>C	GRCh38
NC_000023.10:g.76763884G>C , CM000685.1:g.76763884G>C	GRCh37
NC_000023.9:g.76650540G>C	NCBI36
NG_008838.2:g.282816C>G
NG_008838.3:g.282864C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7424C>G MANE Select	ENSP00000362441.4:p.Ala2475Gly
ENST00000675732.1:c.2522C>G	ENSP00000502598.1:p.Ala841Gly
ENST00000373344.9:c.7424C>G	ENSP00000362441.4:p.Ala2475Gly
ENST00000395603.7:c.7310C>G	ENSP00000378967.3:p.Ala2437Gly
ENST00000480283.5:c.*7052C>G	ENSP00000480196.1:n.*7052C>G
ENST00000623706.3:n.5744C>G
NM_000489.4:c.7424C>G	NP_000480.3:p.Ala2475Gly
NM_138270.3:c.7310C>G	NP_612114.2:p.Ala2437Gly
XM_005262153.3:c.7421C>G	XP_005262210.2:p.Ala2474Gly
XM_005262154.3:c.7337C>G	XP_005262211.2:p.Ala2446Gly
XM_005262155.3:c.7307C>G	XP_005262212.2:p.Ala2436Gly
XM_005262156.3:c.7259C>G	XP_005262213.2:p.Ala2420Gly
XM_005262157.3:c.7220C>G	XP_005262214.2:p.Ala2407Gly
XM_006724666.2:c.7307C>G	XP_006724729.1:p.Ala2436Gly
XM_006724667.2:c.7145C>G	XP_006724730.1:p.Ala2382Gly
XR_938400.1:n.9016C>G
NM_000489.5:c.7424C>G	NP_000480.3:p.Ala2475Gly
XM_005262153.5:c.7421C>G	XP_005262210.2:p.Ala2474Gly
XM_005262154.5:c.7337C>G	XP_005262211.2:p.Ala2446Gly
XM_005262155.4:c.7307C>G	XP_005262212.2:p.Ala2436Gly
XM_005262156.4:c.7259C>G	XP_005262213.2:p.Ala2420Gly
XM_005262157.5:c.7220C>G	XP_005262214.2:p.Ala2407Gly
XM_006724666.4:c.7307C>G	XP_006724729.1:p.Ala2436Gly
XM_006724667.3:c.7145C>G	XP_006724730.1:p.Ala2382Gly
XM_017029601.2:c.7334C>G	XP_016885090.1:p.Ala2445Gly
XM_017029602.1:c.7304C>G	XP_016885091.1:p.Ala2435Gly
XM_017029603.1:c.7256C>G	XP_016885092.1:p.Ala2419Gly
XM_017029604.2:c.7223C>G	XP_016885093.1:p.Ala2408Gly
XM_017029605.1:c.7220C>G	XP_016885094.1:p.Ala2407Gly
XM_017029606.2:c.7193C>G	XP_016885095.1:p.Ala2398Gly
XM_017029607.2:c.7190C>G	XP_016885096.1:p.Ala2397Gly
XM_017029608.2:c.7142C>G	XP_016885097.1:p.Ala2381Gly
XM_017029609.1:c.7106C>G	XP_016885098.1:p.Ala2369Gly
XM_017029610.1:c.7103C>G	XP_016885099.1:p.Ala2368Gly
XM_017029611.1:c.7058C>G	XP_016885100.1:p.Ala2353Gly
XR_001755700.2:n.7723C>G
NM_138270.4:c.7310C>G	NP_612114.2:p.Ala2437Gly
NM_000489.6:c.7424C>G MANE Select	NP_000480.3:p.Ala2475Gly
NM_138270.5:c.7310C>G	NP_612114.2:p.Ala2437Gly