Canonical Allele Identifier: CA2376620

Linked Data

ClinVar Variation Id: 225498
dbSNP Id: rs200773268
gnomAD v2: 3-48508344-G-A
gnomAD v3: 3-48466945-G-A
gnomAD v4: 3-48466945-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466945G>A , CM000665.2:g.48466945G>A GRCh38
NC_000003.11:g.48508344G>A , CM000665.1:g.48508344G>A GRCh37
NC_000003.10:g.48483348G>A NCBI36
NG_009820.1:g.6116G>A
NG_033100.1:g.38916C>T
NG_041782.1:g.25236G>A
NG_009820.2:g.6116G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1391G>A (ATRIP) MANE Select ENSP00000323099.3:n.*1391G>A
ENST00000492235.2:c.-128G>A (TREX1) ENSP00000494511.1:n.-128G>A
ENST00000625293.3:c.290G>A (TREX1) MANE Select ENSP00000486676.2:p.Arg97His
ENST00000634384.2:c.2885G>A (ATRIP)
ENST00000635452.2:c.-128G>A (TREX1) ENSP00000492023.2:n.-128G>A
ENST00000296443.11:c.290G>A ENSP00000296443.11:p.Arg97His
ENST00000433541.1:c.-128G>A (TREX1) ENSP00000412404.1:n.-128G>A
ENST00000444177.1:c.260G>A (TREX1) ENSP00000415972.1:p.Arg87His
ENST00000456089.1:c.-8-120G>A (TREX1) ENSP00000411331.1:n.-8-120G>A
ENST00000492235.1:n.208G>A (TREX1)
ENST00000625293.1:c.455G>A (TREX1) ENSP00000486676.1:p.Arg152His
ENST00000629913.1:c.290G>A (TREX1) ENSP00000486444.1:p.Arg97His
ENST00000634384.1:c.*3110G>A ENSP00000489041.1:n.*3110G>A
ENST00000635452.1:n.1497G>A
ENST00000635464.1:c.3243G>A ENSP00000489199.1:n.3243G>A
NM_007248.3:c.260G>A (TREX1) NP_009179.2:p.Arg87His
NM_016381.5:c.455G>A (TREX1) NP_057465.1:p.Arg152His
NM_033629.4:c.290G>A (TREX1) NP_338599.1:p.Arg97His
NM_007248.4:c.260G>A (TREX1) NP_009179.2:p.Arg87His
NM_033629.5:c.290G>A (TREX1) NP_338599.1:p.Arg97His
NR_153405.1:n.3599G>A
NM_033629.6:c.290G>A (TREX1) MANE Select NP_338599.1:p.Arg97His
NM_130384.3:c.*1391G>A (ATRIP) MANE Select NP_569055.1:n.*1391G>A
NM_001271023.2:c.*1391G>A (ATRIP) NP_001257952.1:n.*1391G>A
NM_007248.5:c.260G>A (TREX1) NP_009179.2:p.Arg87His
NM_032166.4:c.*1391G>A (ATRIP) NP_115542.2:n.*1391G>A
NM_001271022.2:c.*1391G>A (ATRIP) NP_001257951.1:n.*1391G>A