Canonical Allele Identifier: CA413703952

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763914C>A (hg19) ; chrX:g.77508436C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508436C>A , CM000685.2:g.77508436C>A	GRCh38
NC_000023.10:g.76763914C>A , CM000685.1:g.76763914C>A	GRCh37
NC_000023.9:g.76650570C>A	NCBI36
NG_008838.2:g.282786G>T
NG_008838.3:g.282834G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7394G>T MANE Select	ENSP00000362441.4:p.Gly2465Val
ENST00000675732.1:c.2492G>T	ENSP00000502598.1:p.Gly831Val
ENST00000373344.9:c.7394G>T	ENSP00000362441.4:p.Gly2465Val
ENST00000395603.7:c.7280G>T	ENSP00000378967.3:p.Gly2427Val
ENST00000480283.5:c.*7022G>T	ENSP00000480196.1:n.*7022G>T
ENST00000623706.3:n.5714G>T
NM_000489.4:c.7394G>T	NP_000480.3:p.Gly2465Val
NM_138270.3:c.7280G>T	NP_612114.2:p.Gly2427Val
XM_005262153.3:c.7391G>T	XP_005262210.2:p.Gly2464Val
XM_005262154.3:c.7307G>T	XP_005262211.2:p.Gly2436Val
XM_005262155.3:c.7277G>T	XP_005262212.2:p.Gly2426Val
XM_005262156.3:c.7229G>T	XP_005262213.2:p.Gly2410Val
XM_005262157.3:c.7190G>T	XP_005262214.2:p.Gly2397Val
XM_006724666.2:c.7277G>T	XP_006724729.1:p.Gly2426Val
XM_006724667.2:c.7115G>T	XP_006724730.1:p.Gly2372Val
XR_938400.1:n.8986G>T
NM_000489.5:c.7394G>T	NP_000480.3:p.Gly2465Val
XM_005262153.5:c.7391G>T	XP_005262210.2:p.Gly2464Val
XM_005262154.5:c.7307G>T	XP_005262211.2:p.Gly2436Val
XM_005262155.4:c.7277G>T	XP_005262212.2:p.Gly2426Val
XM_005262156.4:c.7229G>T	XP_005262213.2:p.Gly2410Val
XM_005262157.5:c.7190G>T	XP_005262214.2:p.Gly2397Val
XM_006724666.4:c.7277G>T	XP_006724729.1:p.Gly2426Val
XM_006724667.3:c.7115G>T	XP_006724730.1:p.Gly2372Val
XM_017029601.2:c.7304G>T	XP_016885090.1:p.Gly2435Val
XM_017029602.1:c.7274G>T	XP_016885091.1:p.Gly2425Val
XM_017029603.1:c.7226G>T	XP_016885092.1:p.Gly2409Val
XM_017029604.2:c.7193G>T	XP_016885093.1:p.Gly2398Val
XM_017029605.1:c.7190G>T	XP_016885094.1:p.Gly2397Val
XM_017029606.2:c.7163G>T	XP_016885095.1:p.Gly2388Val
XM_017029607.2:c.7160G>T	XP_016885096.1:p.Gly2387Val
XM_017029608.2:c.7112G>T	XP_016885097.1:p.Gly2371Val
XM_017029609.1:c.7076G>T	XP_016885098.1:p.Gly2359Val
XM_017029610.1:c.7073G>T	XP_016885099.1:p.Gly2358Val
XM_017029611.1:c.7028G>T	XP_016885100.1:p.Gly2343Val
XR_001755700.2:n.7693G>T
NM_138270.4:c.7280G>T	NP_612114.2:p.Gly2427Val
NM_000489.6:c.7394G>T MANE Select	NP_000480.3:p.Gly2465Val
NM_138270.5:c.7280G>T	NP_612114.2:p.Gly2427Val