Canonical Allele Identifier: CA413703604

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763870T>C (hg19) ; chrX:g.77508392T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508392T>C , CM000685.2:g.77508392T>C	GRCh38
NC_000023.10:g.76763870T>C , CM000685.1:g.76763870T>C	GRCh37
NC_000023.9:g.76650526T>C	NCBI36
NG_008838.2:g.282830A>G
NG_008838.3:g.282878A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7438A>G MANE Select	ENSP00000362441.4:p.Arg2480Gly
ENST00000675732.1:c.2536A>G	ENSP00000502598.1:p.Arg846Gly
ENST00000373344.9:c.7438A>G	ENSP00000362441.4:p.Arg2480Gly
ENST00000395603.7:c.7324A>G	ENSP00000378967.3:p.Arg2442Gly
ENST00000480283.5:c.*7066A>G	ENSP00000480196.1:n.*7066A>G
ENST00000623706.3:n.5758A>G
NM_000489.4:c.7438A>G	NP_000480.3:p.Arg2480Gly
NM_138270.3:c.7324A>G	NP_612114.2:p.Arg2442Gly
XM_005262153.3:c.7435A>G	XP_005262210.2:p.Arg2479Gly
XM_005262154.3:c.7351A>G	XP_005262211.2:p.Arg2451Gly
XM_005262155.3:c.7321A>G	XP_005262212.2:p.Arg2441Gly
XM_005262156.3:c.7273A>G	XP_005262213.2:p.Arg2425Gly
XM_005262157.3:c.7234A>G	XP_005262214.2:p.Arg2412Gly
XM_006724666.2:c.7321A>G	XP_006724729.1:p.Arg2441Gly
XM_006724667.2:c.7159A>G	XP_006724730.1:p.Arg2387Gly
XR_938400.1:n.9030A>G
NM_000489.5:c.7438A>G	NP_000480.3:p.Arg2480Gly
XM_005262153.5:c.7435A>G	XP_005262210.2:p.Arg2479Gly
XM_005262154.5:c.7351A>G	XP_005262211.2:p.Arg2451Gly
XM_005262155.4:c.7321A>G	XP_005262212.2:p.Arg2441Gly
XM_005262156.4:c.7273A>G	XP_005262213.2:p.Arg2425Gly
XM_005262157.5:c.7234A>G	XP_005262214.2:p.Arg2412Gly
XM_006724666.4:c.7321A>G	XP_006724729.1:p.Arg2441Gly
XM_006724667.3:c.7159A>G	XP_006724730.1:p.Arg2387Gly
XM_017029601.2:c.7348A>G	XP_016885090.1:p.Arg2450Gly
XM_017029602.1:c.7318A>G	XP_016885091.1:p.Arg2440Gly
XM_017029603.1:c.7270A>G	XP_016885092.1:p.Arg2424Gly
XM_017029604.2:c.7237A>G	XP_016885093.1:p.Arg2413Gly
XM_017029605.1:c.7234A>G	XP_016885094.1:p.Arg2412Gly
XM_017029606.2:c.7207A>G	XP_016885095.1:p.Arg2403Gly
XM_017029607.2:c.7204A>G	XP_016885096.1:p.Arg2402Gly
XM_017029608.2:c.7156A>G	XP_016885097.1:p.Arg2386Gly
XM_017029609.1:c.7120A>G	XP_016885098.1:p.Arg2374Gly
XM_017029610.1:c.7117A>G	XP_016885099.1:p.Arg2373Gly
XM_017029611.1:c.7072A>G	XP_016885100.1:p.Arg2358Gly
XR_001755700.2:n.7737A>G
NM_138270.4:c.7324A>G	NP_612114.2:p.Arg2442Gly
NM_000489.6:c.7438A>G MANE Select	NP_000480.3:p.Arg2480Gly
NM_138270.5:c.7324A>G	NP_612114.2:p.Arg2442Gly