Canonical Allele Identifier: CA433616170

Linked Data

ClinVar Variation Id: 2581545
ClinVar RCV Id: RCV003331950
dbSNP Id: rs1433877282
gnomAD v2: 3-48508687-A-G
gnomAD v3: 3-48467288-A-G
gnomAD v4: 3-48467288-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467288A>G , CM000665.2:g.48467288A>G GRCh38
NC_000003.11:g.48508687A>G , CM000665.1:g.48508687A>G GRCh37
NC_000003.10:g.48483691A>G NCBI36
NG_009820.1:g.6459A>G
NG_033100.1:g.38573T>C
NG_041782.1:g.25579A>G
NG_009820.2:g.6459A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1734A>G (ATRIP) MANE Select ENSP00000323099.3:n.*1734A>G
ENST00000492235.2:c.216A>G (TREX1) ENSP00000494511.1:p.Arg72=
ENST00000625293.3:c.633A>G (TREX1) MANE Select ENSP00000486676.2:p.Arg211=
ENST00000634384.2:c.3228A>G (ATRIP)
ENST00000635452.2:c.216A>G (TREX1) ENSP00000492023.2:p.Arg72=
ENST00000296443.11:c.633A>G ENSP00000296443.11:p.Arg211=
ENST00000433541.1:c.216A>G (TREX1) ENSP00000412404.1:p.Arg72=
ENST00000444177.1:c.603A>G (TREX1) ENSP00000415972.1:p.Arg201=
ENST00000456089.1:c.216A>G (TREX1) ENSP00000411331.1:p.Arg72=
ENST00000492235.1:n.551A>G (TREX1)
ENST00000625293.1:c.798A>G (TREX1) ENSP00000486676.1:p.Arg266=
ENST00000629913.1:c.633A>G (TREX1) ENSP00000486444.1:p.Arg211=
ENST00000634384.1:c.*3453A>G ENSP00000489041.1:n.*3453A>G
ENST00000635452.1:n.1840A>G
ENST00000635464.1:c.3586A>G ENSP00000489199.1:n.3586A>G
NM_007248.3:c.603A>G (TREX1) NP_009179.2:p.Arg201=
NM_016381.5:c.798A>G (TREX1) NP_057465.1:p.Arg266=
NM_033629.4:c.633A>G (TREX1) NP_338599.1:p.Arg211=
NM_007248.4:c.603A>G (TREX1) NP_009179.2:p.Arg201=
NM_033629.5:c.633A>G (TREX1) NP_338599.1:p.Arg211=
NR_153405.1:n.3942A>G
NM_033629.6:c.633A>G (TREX1) MANE Select NP_338599.1:p.Arg211=
NM_130384.3:c.*1734A>G (ATRIP) MANE Select NP_569055.1:n.*1734A>G
NM_001271023.2:c.*1734A>G (ATRIP) NP_001257952.1:n.*1734A>G
NM_007248.5:c.603A>G (TREX1) NP_009179.2:p.Arg201=
NM_032166.4:c.*1734A>G (ATRIP) NP_115542.2:n.*1734A>G
NM_001271022.2:c.*1734A>G (ATRIP) NP_001257951.1:n.*1734A>G