Linked Data
ClinVar Variation Id:
4179
ClinVar RCV Id:
RCV000004396
RCV000004397
RCV000388382
RCV000256102
RCV000850611
RCV001266495
RCV002281693
RCV004540989
dbSNP Id:
rs72556554
ExAC:
3:48508395 G / A
gnomAD v2:
3-48508395-G-A
gnomAD v3:
3-48466996-G-A
gnomAD v4:
3-48466996-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.48466996G>A , CM000665.2:g.48466996G>A | GRCh38 |
| NC_000003.11:g.48508395G>A , CM000665.1:g.48508395G>A | GRCh37 |
| NC_000003.10:g.48483399G>A | NCBI36 |
| NG_009820.1:g.6167G>A | |
| NG_033100.1:g.38865C>T | |
| NG_041782.1:g.25287G>A | |
| NG_009820.2:g.6167G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320211.10:c.*1442G>A (ATRIP) MANE Select | ENSP00000323099.3:n.*1442G>A | |
| ENST00000492235.2:c.-77G>A (TREX1) | ENSP00000494511.1:n.-77G>A | |
| ENST00000625293.3:c.341G>A (TREX1) MANE Select | ENSP00000486676.2:p.Arg114His | |
| ENST00000634384.2:c.2936G>A (ATRIP) | ||
| ENST00000635452.2:c.-77G>A (TREX1) | ENSP00000492023.2:n.-77G>A | |
| ENST00000296443.11:c.341G>A | ENSP00000296443.11:p.Arg114His | |
| ENST00000433541.1:c.-77G>A (TREX1) | ENSP00000412404.1:n.-77G>A | |
| ENST00000444177.1:c.311G>A (TREX1) | ENSP00000415972.1:p.Arg104His | |
| ENST00000456089.1:c.-8-69G>A (TREX1) | ENSP00000411331.1:n.-8-69G>A | |
| ENST00000492235.1:n.259G>A (TREX1) | ||
| ENST00000625293.1:c.506G>A (TREX1) | ENSP00000486676.1:p.Arg169His | |
| ENST00000629913.1:c.341G>A (TREX1) | ENSP00000486444.1:p.Arg114His | |
| ENST00000634384.1:c.*3161G>A | ENSP00000489041.1:n.*3161G>A | |
| ENST00000635452.1:n.1548G>A | ||
| ENST00000635464.1:c.3294G>A | ENSP00000489199.1:n.3294G>A | |
| NM_007248.3:c.311G>A (TREX1) | NP_009179.2:p.Arg104His | |
| NM_016381.5:c.506G>A (TREX1) | NP_057465.1:p.Arg169His | |
| NM_033629.4:c.341G>A (TREX1) | NP_338599.1:p.Arg114His | |
| NM_007248.4:c.311G>A (TREX1) | NP_009179.2:p.Arg104His | |
| NM_033629.5:c.341G>A (TREX1) | NP_338599.1:p.Arg114His | |
| NR_153405.1:n.3650G>A | ||
| NM_033629.6:c.341G>A (TREX1) MANE Select | NP_338599.1:p.Arg114His | |
| NM_130384.3:c.*1442G>A (ATRIP) MANE Select | NP_569055.1:n.*1442G>A | |
| NM_001271023.2:c.*1442G>A (ATRIP) | NP_001257952.1:n.*1442G>A | |
| NM_007248.5:c.311G>A (TREX1) | NP_009179.2:p.Arg104His | |
| NM_032166.4:c.*1442G>A (ATRIP) | NP_115542.2:n.*1442G>A | |
| NM_001271022.2:c.*1442G>A (ATRIP) | NP_001257951.1:n.*1442G>A |