Canonical Allele Identifier: CA352618112

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467095T>G , CM000665.2:g.48467095T>G GRCh38
NC_000003.11:g.48508494T>G , CM000665.1:g.48508494T>G GRCh37
NC_000003.10:g.48483498T>G NCBI36
NG_009820.1:g.6266T>G
NG_033100.1:g.38766A>C
NG_041782.1:g.25386T>G
NG_009820.2:g.6266T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1541T>G (ATRIP) MANE Select ENSP00000323099.3:n.*1541T>G
ENST00000492235.2:c.23T>G (TREX1) ENSP00000494511.1:p.Leu8Arg
ENST00000625293.3:c.440T>G (TREX1) MANE Select ENSP00000486676.2:p.Leu147Arg
ENST00000634384.2:c.3035T>G (ATRIP)
ENST00000635452.2:c.23T>G (TREX1) ENSP00000492023.2:p.Leu8Arg
ENST00000296443.11:c.440T>G ENSP00000296443.11:p.Leu147Arg
ENST00000433541.1:c.23T>G (TREX1) ENSP00000412404.1:p.Leu8Arg
ENST00000444177.1:c.410T>G (TREX1) ENSP00000415972.1:p.Leu137Arg
ENST00000456089.1:c.23T>G (TREX1) ENSP00000411331.1:p.Leu8Arg
ENST00000492235.1:n.358T>G (TREX1)
ENST00000625293.1:c.605T>G (TREX1) ENSP00000486676.1:p.Leu202Arg
ENST00000629913.1:c.440T>G (TREX1) ENSP00000486444.1:p.Leu147Arg
ENST00000634384.1:c.*3260T>G ENSP00000489041.1:n.*3260T>G
ENST00000635452.1:n.1647T>G
ENST00000635464.1:c.3393T>G ENSP00000489199.1:n.3393T>G
NM_007248.3:c.410T>G (TREX1) NP_009179.2:p.Leu137Arg
NM_016381.5:c.605T>G (TREX1) NP_057465.1:p.Leu202Arg
NM_033629.4:c.440T>G (TREX1) NP_338599.1:p.Leu147Arg
NM_007248.4:c.410T>G (TREX1) NP_009179.2:p.Leu137Arg
NM_033629.5:c.440T>G (TREX1) NP_338599.1:p.Leu147Arg
NR_153405.1:n.3749T>G
NM_033629.6:c.440T>G (TREX1) MANE Select NP_338599.1:p.Leu147Arg
NM_130384.3:c.*1541T>G (ATRIP) MANE Select NP_569055.1:n.*1541T>G
NM_001271023.2:c.*1541T>G (ATRIP) NP_001257952.1:n.*1541T>G
NM_007248.5:c.410T>G (TREX1) NP_009179.2:p.Leu137Arg
NM_032166.4:c.*1541T>G (ATRIP) NP_115542.2:n.*1541T>G
NM_001271022.2:c.*1541T>G (ATRIP) NP_001257951.1:n.*1541T>G