Canonical Allele Identifier: CA413720961

Gene: ATRX

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77684595T>C , CM000685.2:g.77684595T>C	GRCh38
NC_000023.10:g.76940087T>C , CM000685.1:g.76940087T>C	GRCh37
NC_000023.9:g.76826743T>C	NCBI36
NG_008838.2:g.106627A>G
NG_008838.3:g.106675A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.663-2A>G MANE Select	ENSP00000362441.4:n.663-2A>G
ENST00000373344.9:c.663-2A>G	ENSP00000362441.4:n.663-2A>G
ENST00000395603.7:c.549-2A>G	ENSP00000378967.3:n.549-2A>G
ENST00000480283.5:c.*291-2A>G	ENSP00000480196.1:n.*291-2A>G
ENST00000623321.3:c.498-2A>G	ENSP00000485127.1:n.498-2A>G
ENST00000624032.3:c.663-2A>G	ENSP00000485253.1:n.663-2A>G
ENST00000624166.3:c.546-2A>G	ENSP00000485103.1:n.546-2A>G
ENST00000625063.3:c.478-2A>G
NM_000489.4:c.663-2A>G	NP_000480.3:n.663-2A>G
NM_138270.3:c.549-2A>G	NP_612114.2:n.549-2A>G
XM_005262153.3:c.660-2A>G	XP_005262210.2:n.660-2A>G
XM_005262154.3:c.663-2A>G	XP_005262211.2:n.663-2A>G
XM_005262155.3:c.546-2A>G	XP_005262212.2:n.546-2A>G
XM_005262156.3:c.498-2A>G	XP_005262213.2:n.498-2A>G
XM_005262157.3:c.546-2A>G	XP_005262214.2:n.546-2A>G
XM_006724666.2:c.546-2A>G	XP_006724729.1:n.546-2A>G
XM_006724667.2:c.384-2A>G	XP_006724730.1:n.384-2A>G
XM_006724668.2:c.663-2A>G	XP_006724731.1:n.663-2A>G
XR_938400.1:n.931-2A>G
NM_000489.5:c.663-2A>G	NP_000480.3:n.663-2A>G
XM_005262153.5:c.660-2A>G	XP_005262210.2:n.660-2A>G
XM_005262154.5:c.663-2A>G	XP_005262211.2:n.663-2A>G
XM_005262155.4:c.546-2A>G	XP_005262212.2:n.546-2A>G
XM_005262156.4:c.498-2A>G	XP_005262213.2:n.498-2A>G
XM_005262157.5:c.546-2A>G	XP_005262214.2:n.546-2A>G
XM_006724666.4:c.546-2A>G	XP_006724729.1:n.546-2A>G
XM_006724667.3:c.384-2A>G	XP_006724730.1:n.384-2A>G
XM_006724668.3:c.663-2A>G	XP_006724731.1:n.663-2A>G
XM_017029601.2:c.660-2A>G	XP_016885090.1:n.660-2A>G
XM_017029602.1:c.543-2A>G	XP_016885091.1:n.543-2A>G
XM_017029603.1:c.495-2A>G	XP_016885092.1:n.495-2A>G
XM_017029604.2:c.549-2A>G	XP_016885093.1:n.549-2A>G
XM_017029605.1:c.546-2A>G	XP_016885094.1:n.546-2A>G
XM_017029606.2:c.432-2A>G	XP_016885095.1:n.432-2A>G
XM_017029607.2:c.429-2A>G	XP_016885096.1:n.429-2A>G
XM_017029608.2:c.381-2A>G	XP_016885097.1:n.381-2A>G
XM_017029609.1:c.432-2A>G	XP_016885098.1:n.432-2A>G
XM_017029610.1:c.429-2A>G	XP_016885099.1:n.429-2A>G
XM_017029611.1:c.384-2A>G	XP_016885100.1:n.384-2A>G
XR_001755700.2:n.888-2A>G
NM_138270.4:c.549-2A>G	NP_612114.2:n.549-2A>G
NM_000489.6:c.663-2A>G MANE Select	NP_000480.3:n.663-2A>G
NM_138270.5:c.549-2A>G	NP_612114.2:n.549-2A>G