Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155461220_155461221delinsTG , CM000669.2:g.155461220_155461221delinsTG | GRCh38 |
| NC_000007.13:g.155253915_155253916delinsTG , CM000669.1:g.155253915_155253916delinsTG | GRCh37 |
| NC_000007.12:g.154946676_154946677delinsTG | NCBI36 |
| NG_007124.1:g.9501_9502delinsTG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000297375.4:c.686-1151_686-1150delinsTG MANE Select | ENSP00000297375.4:n.686-1151_686-1150deli... | |
| NM_001427.3:c.686-1151_686-1150delinsTG | NP_001418.2:n.686-1151_686-1150delinsTG | |
| NM_001427.4:c.686-1151_686-1150delinsTG MANE Select | NP_001418.2:n.686-1151_686-1150delinsTG |