Canonical Allele Identifier: CA413704025

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763930A>C (hg19) ; chrX:g.77508452A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508452A>C , CM000685.2:g.77508452A>C	GRCh38
NC_000023.10:g.76763930A>C , CM000685.1:g.76763930A>C	GRCh37
NC_000023.9:g.76650586A>C	NCBI36
NG_008838.2:g.282770T>G
NG_008838.3:g.282818T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7378T>G MANE Select	ENSP00000362441.4:p.Tyr2460Asp
ENST00000675732.1:c.2476T>G	ENSP00000502598.1:p.Tyr826Asp
ENST00000373344.9:c.7378T>G	ENSP00000362441.4:p.Tyr2460Asp
ENST00000395603.7:c.7264T>G	ENSP00000378967.3:p.Tyr2422Asp
ENST00000480283.5:c.*7006T>G	ENSP00000480196.1:n.*7006T>G
ENST00000623706.3:n.5698T>G
NM_000489.4:c.7378T>G	NP_000480.3:p.Tyr2460Asp
NM_138270.3:c.7264T>G	NP_612114.2:p.Tyr2422Asp
XM_005262153.3:c.7375T>G	XP_005262210.2:p.Tyr2459Asp
XM_005262154.3:c.7291T>G	XP_005262211.2:p.Tyr2431Asp
XM_005262155.3:c.7261T>G	XP_005262212.2:p.Tyr2421Asp
XM_005262156.3:c.7213T>G	XP_005262213.2:p.Tyr2405Asp
XM_005262157.3:c.7174T>G	XP_005262214.2:p.Tyr2392Asp
XM_006724666.2:c.7261T>G	XP_006724729.1:p.Tyr2421Asp
XM_006724667.2:c.7099T>G	XP_006724730.1:p.Tyr2367Asp
XR_938400.1:n.8970T>G
NM_000489.5:c.7378T>G	NP_000480.3:p.Tyr2460Asp
XM_005262153.5:c.7375T>G	XP_005262210.2:p.Tyr2459Asp
XM_005262154.5:c.7291T>G	XP_005262211.2:p.Tyr2431Asp
XM_005262155.4:c.7261T>G	XP_005262212.2:p.Tyr2421Asp
XM_005262156.4:c.7213T>G	XP_005262213.2:p.Tyr2405Asp
XM_005262157.5:c.7174T>G	XP_005262214.2:p.Tyr2392Asp
XM_006724666.4:c.7261T>G	XP_006724729.1:p.Tyr2421Asp
XM_006724667.3:c.7099T>G	XP_006724730.1:p.Tyr2367Asp
XM_017029601.2:c.7288T>G	XP_016885090.1:p.Tyr2430Asp
XM_017029602.1:c.7258T>G	XP_016885091.1:p.Tyr2420Asp
XM_017029603.1:c.7210T>G	XP_016885092.1:p.Tyr2404Asp
XM_017029604.2:c.7177T>G	XP_016885093.1:p.Tyr2393Asp
XM_017029605.1:c.7174T>G	XP_016885094.1:p.Tyr2392Asp
XM_017029606.2:c.7147T>G	XP_016885095.1:p.Tyr2383Asp
XM_017029607.2:c.7144T>G	XP_016885096.1:p.Tyr2382Asp
XM_017029608.2:c.7096T>G	XP_016885097.1:p.Tyr2366Asp
XM_017029609.1:c.7060T>G	XP_016885098.1:p.Tyr2354Asp
XM_017029610.1:c.7057T>G	XP_016885099.1:p.Tyr2353Asp
XM_017029611.1:c.7012T>G	XP_016885100.1:p.Tyr2338Asp
XR_001755700.2:n.7677T>G
NM_138270.4:c.7264T>G	NP_612114.2:p.Tyr2422Asp
NM_000489.6:c.7378T>G MANE Select	NP_000480.3:p.Tyr2460Asp
NM_138270.5:c.7264T>G	NP_612114.2:p.Tyr2422Asp