Linked Data
gnomAD v2:
17-45361771-G-GCCGTATCATTA
MyVariant Identifiers:
chr17:g.45361771_45361772insCCGTATCATTA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47284405_47284406insCCGTATCATTA , CM000679.2:g.47284405_47284406insCCGTATCATTA | GRCh38 |
| NC_000017.10:g.45361771_45361772insCCGTATCATTA , CM000679.1:g.45361771_45361772insCCGTATCATTA | GRCh37 |
| NC_000017.9:g.42716770_42716771insCCGTATCATTA | NCBI36 |
| NG_008332.2:g.35564_35565insCCGTATCATTA , LRG_481:g.35564_35565insCCGTATCATTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.362-38_362-37insCCGTATCATTA | ENSP00000513002.1:n.362-38_362-37insCCGTATCATTA | |
| ENST00000559488.7:c.362-38_362-37insCCGTATCATTA MANE Select | ENSP00000452786.2:n.362-38_362-37insCCGTATCATTA | |
| ENST00000559488.5:c.362-38_362-37insCCGTATCATTA | ENSP00000452786.1:n.362-38_362-37insCCGTATCATTA | |
| ENST00000560629.1:c.327-38_327-37insCCGTATCATTA | ||
| ENST00000571680.1:c.362-38_362-37insCCGTATCATTA | ENSP00000461626.1:n.362-38_362-37insCCGTATCATTA | |
| NM_000212.2:c.362-38_362-37insCCGTATCATTA , LRG_481t1:c.362-38_362-37insCCGTATCATTA | NP_000203.2:n.362-38_362-37insCCGTATCATTA | |
| NM_000212.3:c.362-38_362-37insCCGTATCATTA MANE Select | NP_000203.2:n.362-38_362-37insCCGTATCATTA |