Canonical Allele Identifier:
CA920480111
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.624389_624390insGTG , CM000686.2:g.624389_624390insGTG | GRCh38 |
| NC_000024.9:g.535124_535125insGTG , CM000686.1:g.535124_535125insGTG | GRCh37 |
| NC_000024.8:g.505124_505125insGTG | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000711143.1:c.-646_-645insGTG | ENSP00000518641.1:n.-646_-645insGTG | |
| ENST00000711145.1:c.-646_-645insGTG | ENSP00000518642.1:n.-646_-645insGTG |