Canonical Allele Identifier: CA413704537

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763996T>C (hg19) ; chrX:g.77508518T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508518T>C , CM000685.2:g.77508518T>C	GRCh38
NC_000023.10:g.76763996T>C , CM000685.1:g.76763996T>C	GRCh37
NC_000023.9:g.76650652T>C	NCBI36
NG_008838.2:g.282704A>G
NG_008838.3:g.282752A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7312A>G MANE Select	ENSP00000362441.4:p.Met2438Val
ENST00000675732.1:c.2410A>G	ENSP00000502598.1:p.Met804Val
ENST00000373344.9:c.7312A>G	ENSP00000362441.4:p.Met2438Val
ENST00000395603.7:c.7198A>G	ENSP00000378967.3:p.Met2400Val
ENST00000480283.5:c.*6940A>G	ENSP00000480196.1:n.*6940A>G
ENST00000623706.3:n.5632A>G
ENST00000624766.1:n.543A>G
NM_000489.4:c.7312A>G	NP_000480.3:p.Met2438Val
NM_138270.3:c.7198A>G	NP_612114.2:p.Met2400Val
XM_005262153.3:c.7309A>G	XP_005262210.2:p.Met2437Val
XM_005262154.3:c.7225A>G	XP_005262211.2:p.Met2409Val
XM_005262155.3:c.7195A>G	XP_005262212.2:p.Met2399Val
XM_005262156.3:c.7147A>G	XP_005262213.2:p.Met2383Val
XM_005262157.3:c.7108A>G	XP_005262214.2:p.Met2370Val
XM_006724666.2:c.7195A>G	XP_006724729.1:p.Met2399Val
XM_006724667.2:c.7033A>G	XP_006724730.1:p.Met2345Val
XR_938400.1:n.8904A>G
NM_000489.5:c.7312A>G	NP_000480.3:p.Met2438Val
XM_005262153.5:c.7309A>G	XP_005262210.2:p.Met2437Val
XM_005262154.5:c.7225A>G	XP_005262211.2:p.Met2409Val
XM_005262155.4:c.7195A>G	XP_005262212.2:p.Met2399Val
XM_005262156.4:c.7147A>G	XP_005262213.2:p.Met2383Val
XM_005262157.5:c.7108A>G	XP_005262214.2:p.Met2370Val
XM_006724666.4:c.7195A>G	XP_006724729.1:p.Met2399Val
XM_006724667.3:c.7033A>G	XP_006724730.1:p.Met2345Val
XM_017029601.2:c.7222A>G	XP_016885090.1:p.Met2408Val
XM_017029602.1:c.7192A>G	XP_016885091.1:p.Met2398Val
XM_017029603.1:c.7144A>G	XP_016885092.1:p.Met2382Val
XM_017029604.2:c.7111A>G	XP_016885093.1:p.Met2371Val
XM_017029605.1:c.7108A>G	XP_016885094.1:p.Met2370Val
XM_017029606.2:c.7081A>G	XP_016885095.1:p.Met2361Val
XM_017029607.2:c.7078A>G	XP_016885096.1:p.Met2360Val
XM_017029608.2:c.7030A>G	XP_016885097.1:p.Met2344Val
XM_017029609.1:c.6994A>G	XP_016885098.1:p.Met2332Val
XM_017029610.1:c.6991A>G	XP_016885099.1:p.Met2331Val
XM_017029611.1:c.6946A>G	XP_016885100.1:p.Met2316Val
XR_001755700.2:n.7611A>G
NM_138270.4:c.7198A>G	NP_612114.2:p.Met2400Val
NM_000489.6:c.7312A>G MANE Select	NP_000480.3:p.Met2438Val
NM_138270.5:c.7198A>G	NP_612114.2:p.Met2400Val