Canonical Allele Identifier: CA277098

Gene: ATRX

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77635992_77635997del , CM000685.2:g.77635992_77635997del	GRCh38
NC_000023.10:g.76891483_76891488del , CM000685.1:g.76891483_76891488del	GRCh37
NC_000023.9:g.76778139_76778144del	NCBI36
NG_008838.2:g.155234_155239del
NG_008838.3:g.155282_155287del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4626_4631del MANE Select	ENSP00000362441.4:p.Asp1542_Glu1543del
ENST00000373344.9:c.4626_4631del	ENSP00000362441.4:p.Asp1542_Glu1543del
ENST00000395603.7:c.4512_4517del	ENSP00000378967.3:p.Asp1504_Glu1505del
ENST00000460639.2:n.106_111del
ENST00000480283.5:c.*4254_*4259del	ENSP00000480196.1:n.*4254_*4259del
ENST00000623242.3:c.363_368del
NM_000489.4:c.4626_4631del	NP_000480.3:p.Asp1542_Glu1543del
NM_138270.3:c.4512_4517del	NP_612114.2:p.Asp1504_Glu1505del
XM_005262153.3:c.4623_4628del	XP_005262210.2:p.Asp1541_Glu1542del
XM_005262154.3:c.4539_4544del	XP_005262211.2:p.Asp1513_Glu1514del
XM_005262155.3:c.4509_4514del	XP_005262212.2:p.Asp1503_Glu1504del
XM_005262156.3:c.4461_4466del	XP_005262213.2:p.Asp1487_Glu1488del
XM_005262157.3:c.4422_4427del	XP_005262214.2:p.Asp1474_Glu1475del
XM_006724666.2:c.4509_4514del	XP_006724729.1:p.Asp1503_Glu1504del
XM_006724667.2:c.4347_4352del	XP_006724730.1:p.Asp1449_Glu1450del
XM_006724668.2:c.4626_4631del	XP_006724731.1:p.Asp1542_Glu1543del
XR_938400.1:n.4894_4899del
NM_000489.5:c.4626_4631del	NP_000480.3:p.Asp1542_Glu1543del
XM_005262153.5:c.4623_4628del	XP_005262210.2:p.Asp1541_Glu1542del
XM_005262154.5:c.4539_4544del	XP_005262211.2:p.Asp1513_Glu1514del
XM_005262155.4:c.4509_4514del	XP_005262212.2:p.Asp1503_Glu1504del
XM_005262156.4:c.4461_4466del	XP_005262213.2:p.Asp1487_Glu1488del
XM_005262157.5:c.4422_4427del	XP_005262214.2:p.Asp1474_Glu1475del
XM_006724666.4:c.4509_4514del	XP_006724729.1:p.Asp1503_Glu1504del
XM_006724667.3:c.4347_4352del	XP_006724730.1:p.Asp1449_Glu1450del
XM_006724668.3:c.4626_4631del	XP_006724731.1:p.Asp1542_Glu1543del
XM_017029601.2:c.4536_4541del	XP_016885090.1:p.Asp1512_Glu1513del
XM_017029602.1:c.4506_4511del	XP_016885091.1:p.Asp1502_Glu1503del
XM_017029603.1:c.4458_4463del	XP_016885092.1:p.Asp1486_Glu1487del
XM_017029604.2:c.4425_4430del	XP_016885093.1:p.Asp1475_Glu1476del
XM_017029605.1:c.4422_4427del	XP_016885094.1:p.Asp1474_Glu1475del
XM_017029606.2:c.4395_4400del	XP_016885095.1:p.Asp1465_Glu1466del
XM_017029607.2:c.4392_4397del	XP_016885096.1:p.Asp1464_Glu1465del
XM_017029608.2:c.4344_4349del	XP_016885097.1:p.Asp1448_Glu1449del
XM_017029609.1:c.4308_4313del	XP_016885098.1:p.Asp1436_Glu1437del
XM_017029610.1:c.4305_4310del	XP_016885099.1:p.Asp1435_Glu1436del
XM_017029611.1:c.4260_4265del	XP_016885100.1:p.Asp1420_Glu1421del
XR_001755700.2:n.4851_4856del
NM_138270.4:c.4512_4517del	NP_612114.2:p.Asp1504_Glu1505del
NM_000489.6:c.4626_4631del MANE Select	NP_000480.3:p.Asp1542_Glu1543del
NM_138270.5:c.4512_4517del	NP_612114.2:p.Asp1504_Glu1505del