Canonical Allele Identifier: CA2438929041

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508435_77508436delinsAC , CM000685.2:g.77508435_77508436delinsAC	GRCh38
NC_000023.10:g.76763913_76763914delinsAC , CM000685.1:g.76763913_76763914delinsAC	GRCh37
NC_000023.9:g.76650569_76650570delinsAC	NCBI36
NG_008838.2:g.282786_282787delinsGT
NG_008838.3:g.282834_282835delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7394_7395delinsGT MANE Select	ENSP00000362441.4:p.Gly2465=
ENST00000675732.1:c.2492_2493delinsGT	ENSP00000502598.1:p.Gly831=
ENST00000373344.9:c.7394_7395delinsGT	ENSP00000362441.4:p.Gly2465=
ENST00000395603.7:c.7280_7281delinsGT	ENSP00000378967.3:p.Gly2427=
ENST00000480283.5:c.*7022_*7023delinsGT	ENSP00000480196.1:n.*7022_*7023delinsGT
ENST00000623706.3:n.5714_5715delinsGT
NM_000489.4:c.7394_7395delinsGT	NP_000480.3:p.Gly2465=
NM_138270.3:c.7280_7281delinsGT	NP_612114.2:p.Gly2427=
XM_005262153.3:c.7391_7392delinsGT	XP_005262210.2:p.Gly2464=
XM_005262154.3:c.7307_7308delinsGT	XP_005262211.2:p.Gly2436=
XM_005262155.3:c.7277_7278delinsGT	XP_005262212.2:p.Gly2426=
XM_005262156.3:c.7229_7230delinsGT	XP_005262213.2:p.Gly2410=
XM_005262157.3:c.7190_7191delinsGT	XP_005262214.2:p.Gly2397=
XM_006724666.2:c.7277_7278delinsGT	XP_006724729.1:p.Gly2426=
XM_006724667.2:c.7115_7116delinsGT	XP_006724730.1:p.Gly2372=
XR_938400.1:n.8986_8987delinsGT
NM_000489.5:c.7394_7395delinsGT	NP_000480.3:p.Gly2465=
XM_005262153.5:c.7391_7392delinsGT	XP_005262210.2:p.Gly2464=
XM_005262154.5:c.7307_7308delinsGT	XP_005262211.2:p.Gly2436=
XM_005262155.4:c.7277_7278delinsGT	XP_005262212.2:p.Gly2426=
XM_005262156.4:c.7229_7230delinsGT	XP_005262213.2:p.Gly2410=
XM_005262157.5:c.7190_7191delinsGT	XP_005262214.2:p.Gly2397=
XM_006724666.4:c.7277_7278delinsGT	XP_006724729.1:p.Gly2426=
XM_006724667.3:c.7115_7116delinsGT	XP_006724730.1:p.Gly2372=
XM_017029601.2:c.7304_7305delinsGT	XP_016885090.1:p.Gly2435=
XM_017029602.1:c.7274_7275delinsGT	XP_016885091.1:p.Gly2425=
XM_017029603.1:c.7226_7227delinsGT	XP_016885092.1:p.Gly2409=
XM_017029604.2:c.7193_7194delinsGT	XP_016885093.1:p.Gly2398=
XM_017029605.1:c.7190_7191delinsGT	XP_016885094.1:p.Gly2397=
XM_017029606.2:c.7163_7164delinsGT	XP_016885095.1:p.Gly2388=
XM_017029607.2:c.7160_7161delinsGT	XP_016885096.1:p.Gly2387=
XM_017029608.2:c.7112_7113delinsGT	XP_016885097.1:p.Gly2371=
XM_017029609.1:c.7076_7077delinsGT	XP_016885098.1:p.Gly2359=
XM_017029610.1:c.7073_7074delinsGT	XP_016885099.1:p.Gly2358=
XM_017029611.1:c.7028_7029delinsGT	XP_016885100.1:p.Gly2343=
XR_001755700.2:n.7693_7694delinsGT
NM_138270.4:c.7280_7281delinsGT	NP_612114.2:p.Gly2427=
NM_000489.6:c.7394_7395delinsGT MANE Select	NP_000480.3:p.Gly2465=
NM_138270.5:c.7280_7281delinsGT	NP_612114.2:p.Gly2427=