Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190416_204190417insAA , CM000663.2:g.204190416_204190417insAA | GRCh38 |
| NC_000001.10:g.204159544_204159545insAA , CM000663.1:g.204159544_204159545insAA | GRCh37 |
| NC_000001.9:g.202426167_202426168insAA | NCBI36 |
| NG_032151.1:g.11075_11076insTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.*67_*68insTT MANE Select | ENSP00000356162.4:n.*67_*68insTT | |
| ENST00000367194.4:c.*67_*68insTT | ENSP00000356162.4:n.*67_*68insTT | |
| NM_002256.3:c.*67_*68insTT | NP_002247.3:n.*67_*68insTT | |
| XM_011509525.1:c.*67_*68insTT | XP_011507827.1:n.*67_*68insTT | |
| NM_002256.4:c.*67_*68insTT MANE Select | NP_002247.3:n.*67_*68insTT |