Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74749515_74749519delinsATCTT , CM000677.2:g.74749515_74749519delinsATCTT | GRCh38 |
| NC_000015.9:g.75041856_75041860delinsATCTT , CM000677.1:g.75041856_75041860delinsATCTT | GRCh37 |
| NC_000015.8:g.72828909_72828913delinsATCTT | NCBI36 |
| NG_008431.1:g.31974_31978delinsATCTT | |
| NG_008431.2:g.31974_31978delinsATCTT | |
| NG_061543.1:g.5671_5675delinsATCTT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343932.5:c.-9-215_-9-211delinsATCTT MANE Select | ENSP00000342007.4:n.-9-215_-9-211delinsAT... | |
| ENST00000343932.4:c.-9-215_-9-211delinsATCTT | ENSP00000342007.4:n.-9-215_-9-211delinsAT... | |
| NM_000761.4:c.-9-215_-9-211delinsATCTT | NP_000752.2:n.-9-215_-9-211delinsATCTT | |
| NM_000761.5:c.-9-215_-9-211delinsATCTT MANE Select | NP_000752.2:n.-9-215_-9-211delinsATCTT |