Canonical Allele Identifier: CA276175

Linked Data

ClinVar Variation Id: 209198
dbSNP Id: rs760838030
gnomAD v2: 3-48508394-C-T
gnomAD v3: 3-48466995-C-T
gnomAD v4: 3-48466995-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466995C>T , CM000665.2:g.48466995C>T GRCh38
NC_000003.11:g.48508394C>T , CM000665.1:g.48508394C>T GRCh37
NC_000003.10:g.48483398C>T NCBI36
NG_009820.1:g.6166C>T
NG_033100.1:g.38866G>A
NG_041782.1:g.25286C>T
NG_009820.2:g.6166C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1441C>T (ATRIP) MANE Select ENSP00000323099.3:n.*1441C>T
ENST00000492235.2:c.-78C>T (TREX1) ENSP00000494511.1:n.-78C>T
ENST00000625293.3:c.340C>T (TREX1) MANE Select ENSP00000486676.2:p.Arg114Cys
ENST00000634384.2:c.2935C>T (ATRIP)
ENST00000635452.2:c.-78C>T (TREX1) ENSP00000492023.2:n.-78C>T
ENST00000296443.11:c.340C>T ENSP00000296443.11:p.Arg114Cys
ENST00000433541.1:c.-78C>T (TREX1) ENSP00000412404.1:n.-78C>T
ENST00000444177.1:c.310C>T (TREX1) ENSP00000415972.1:p.Arg104Cys
ENST00000456089.1:c.-8-70C>T (TREX1) ENSP00000411331.1:n.-8-70C>T
ENST00000492235.1:n.258C>T (TREX1)
ENST00000625293.1:c.505C>T (TREX1) ENSP00000486676.1:p.Arg169Cys
ENST00000629913.1:c.340C>T (TREX1) ENSP00000486444.1:p.Arg114Cys
ENST00000634384.1:c.*3160C>T ENSP00000489041.1:n.*3160C>T
ENST00000635452.1:n.1547C>T
ENST00000635464.1:c.3293C>T ENSP00000489199.1:n.3293C>T
NM_007248.3:c.310C>T (TREX1) NP_009179.2:p.Arg104Cys
NM_016381.5:c.505C>T (TREX1) NP_057465.1:p.Arg169Cys
NM_033629.4:c.340C>T (TREX1) NP_338599.1:p.Arg114Cys
NM_007248.4:c.310C>T (TREX1) NP_009179.2:p.Arg104Cys
NM_033629.5:c.340C>T (TREX1) NP_338599.1:p.Arg114Cys
NR_153405.1:n.3649C>T
NM_033629.6:c.340C>T (TREX1) MANE Select NP_338599.1:p.Arg114Cys
NM_130384.3:c.*1441C>T (ATRIP) MANE Select NP_569055.1:n.*1441C>T
NM_001271023.2:c.*1441C>T (ATRIP) NP_001257952.1:n.*1441C>T
NM_007248.5:c.310C>T (TREX1) NP_009179.2:p.Arg104Cys
NM_032166.4:c.*1441C>T (ATRIP) NP_115542.2:n.*1441C>T
NM_001271022.2:c.*1441C>T (ATRIP) NP_001257951.1:n.*1441C>T