Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190411_204190412insGC , CM000663.2:g.204190411_204190412insGC | GRCh38 |
| NC_000001.10:g.204159539_204159540insGC , CM000663.1:g.204159539_204159540insGC | GRCh37 |
| NC_000001.9:g.202426162_202426163insGC | NCBI36 |
| NG_032151.1:g.11081_11082insCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.*73_*74insCG MANE Select | ENSP00000356162.4:n.*73_*74insCG | |
| ENST00000367194.4:c.*73_*74insCG | ENSP00000356162.4:n.*73_*74insCG | |
| NM_002256.3:c.*73_*74insCG | NP_002247.3:n.*73_*74insCG | |
| XM_011509525.1:c.*73_*74insCG | XP_011507827.1:n.*73_*74insCG | |
| NM_002256.4:c.*73_*74insCG MANE Select | NP_002247.3:n.*73_*74insCG |