Canonical Allele Identifier: CA352618274

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467151A>T , CM000665.2:g.48467151A>T GRCh38
NC_000003.11:g.48508550A>T , CM000665.1:g.48508550A>T GRCh37
NC_000003.10:g.48483554A>T NCBI36
NG_009820.1:g.6322A>T
NG_033100.1:g.38710T>A
NG_041782.1:g.25442A>T
NG_009820.2:g.6322A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320211.10:c.*1597A>T (ATRIP) MANE Select ENSP00000323099.3:n.*1597A>T
ENST00000492235.2:c.79A>T (TREX1) ENSP00000494511.1:p.Ser27Cys
ENST00000625293.3:c.496A>T (TREX1) MANE Select ENSP00000486676.2:p.Ser166Cys
ENST00000634384.2:c.3091A>T (ATRIP)
ENST00000635452.2:c.79A>T (TREX1) ENSP00000492023.2:p.Ser27Cys
ENST00000296443.11:c.496A>T ENSP00000296443.11:p.Ser166Cys
ENST00000433541.1:c.79A>T (TREX1) ENSP00000412404.1:p.Ser27Cys
ENST00000444177.1:c.466A>T (TREX1) ENSP00000415972.1:p.Ser156Cys
ENST00000456089.1:c.79A>T (TREX1) ENSP00000411331.1:p.Ser27Cys
ENST00000492235.1:n.414A>T (TREX1)
ENST00000625293.1:c.661A>T (TREX1) ENSP00000486676.1:p.Ser221Cys
ENST00000629913.1:c.496A>T (TREX1) ENSP00000486444.1:p.Ser166Cys
ENST00000634384.1:c.*3316A>T ENSP00000489041.1:n.*3316A>T
ENST00000635452.1:n.1703A>T
ENST00000635464.1:c.3449A>T ENSP00000489199.1:n.3449A>T
NM_007248.3:c.466A>T (TREX1) NP_009179.2:p.Ser156Cys
NM_016381.5:c.661A>T (TREX1) NP_057465.1:p.Ser221Cys
NM_033629.4:c.496A>T (TREX1) NP_338599.1:p.Ser166Cys
NM_007248.4:c.466A>T (TREX1) NP_009179.2:p.Ser156Cys
NM_033629.5:c.496A>T (TREX1) NP_338599.1:p.Ser166Cys
NR_153405.1:n.3805A>T
NM_033629.6:c.496A>T (TREX1) MANE Select NP_338599.1:p.Ser166Cys
NM_130384.3:c.*1597A>T (ATRIP) MANE Select NP_569055.1:n.*1597A>T
NM_001271023.2:c.*1597A>T (ATRIP) NP_001257952.1:n.*1597A>T
NM_007248.5:c.466A>T (TREX1) NP_009179.2:p.Ser156Cys
NM_032166.4:c.*1597A>T (ATRIP) NP_115542.2:n.*1597A>T
NM_001271022.2:c.*1597A>T (ATRIP) NP_001257951.1:n.*1597A>T