Canonical Allele Identifier: CA517374072

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763937T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508459T>C , CM000685.2:g.77508459T>C	GRCh38
NC_000023.10:g.76763937T>C , CM000685.1:g.76763937T>C	GRCh37
NC_000023.9:g.76650593T>C	NCBI36
NG_008838.2:g.282763A>G
NG_008838.3:g.282811A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7371A>G MANE Select	ENSP00000362441.4:p.Arg2457=
ENST00000675732.1:c.2469A>G	ENSP00000502598.1:p.Arg823=
ENST00000373344.9:c.7371A>G	ENSP00000362441.4:p.Arg2457=
ENST00000395603.7:c.7257A>G	ENSP00000378967.3:p.Arg2419=
ENST00000480283.5:c.*6999A>G	ENSP00000480196.1:n.*6999A>G
ENST00000623706.3:n.5691A>G
NM_000489.4:c.7371A>G	NP_000480.3:p.Arg2457=
NM_138270.3:c.7257A>G	NP_612114.2:p.Arg2419=
XM_005262153.3:c.7368A>G	XP_005262210.2:p.Arg2456=
XM_005262154.3:c.7284A>G	XP_005262211.2:p.Arg2428=
XM_005262155.3:c.7254A>G	XP_005262212.2:p.Arg2418=
XM_005262156.3:c.7206A>G	XP_005262213.2:p.Arg2402=
XM_005262157.3:c.7167A>G	XP_005262214.2:p.Arg2389=
XM_006724666.2:c.7254A>G	XP_006724729.1:p.Arg2418=
XM_006724667.2:c.7092A>G	XP_006724730.1:p.Arg2364=
XR_938400.1:n.8963A>G
NM_000489.5:c.7371A>G	NP_000480.3:p.Arg2457=
XM_005262153.5:c.7368A>G	XP_005262210.2:p.Arg2456=
XM_005262154.5:c.7284A>G	XP_005262211.2:p.Arg2428=
XM_005262155.4:c.7254A>G	XP_005262212.2:p.Arg2418=
XM_005262156.4:c.7206A>G	XP_005262213.2:p.Arg2402=
XM_005262157.5:c.7167A>G	XP_005262214.2:p.Arg2389=
XM_006724666.4:c.7254A>G	XP_006724729.1:p.Arg2418=
XM_006724667.3:c.7092A>G	XP_006724730.1:p.Arg2364=
XM_017029601.2:c.7281A>G	XP_016885090.1:p.Arg2427=
XM_017029602.1:c.7251A>G	XP_016885091.1:p.Arg2417=
XM_017029603.1:c.7203A>G	XP_016885092.1:p.Arg2401=
XM_017029604.2:c.7170A>G	XP_016885093.1:p.Arg2390=
XM_017029605.1:c.7167A>G	XP_016885094.1:p.Arg2389=
XM_017029606.2:c.7140A>G	XP_016885095.1:p.Arg2380=
XM_017029607.2:c.7137A>G	XP_016885096.1:p.Arg2379=
XM_017029608.2:c.7089A>G	XP_016885097.1:p.Arg2363=
XM_017029609.1:c.7053A>G	XP_016885098.1:p.Arg2351=
XM_017029610.1:c.7050A>G	XP_016885099.1:p.Arg2350=
XM_017029611.1:c.7005A>G	XP_016885100.1:p.Arg2335=
XR_001755700.2:n.7670A>G
NM_138270.4:c.7257A>G	NP_612114.2:p.Arg2419=
NM_000489.6:c.7371A>G MANE Select	NP_000480.3:p.Arg2457=
NM_138270.5:c.7257A>G	NP_612114.2:p.Arg2419=