Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118111660_118111661delinsCG , CM000670.2:g.118111660_118111661delinsCG | GRCh38 |
| NC_000008.10:g.119123899_119123900delinsCG , CM000670.1:g.119123899_119123900delinsCG | GRCh37 |
| NC_000008.9:g.119193080_119193081delinsCG | NCBI36 |
| NG_007455.2:g.5159_5160delinsCG , LRG_493:g.5159_5160delinsCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378204.7:c.-615_-614delinsCG MANE Select | ENSP00000367446.3:n.-615_-614delinsCG | |
| ENST00000378204.6:c.-615_-614delinsCG | ENSP00000367446.2:n.-615_-614delinsCG | |
| NM_000127.2:c.-615_-614delinsCG , LRG_493t1:c.-615_-614delinsCG | NP_000118.2:n.-615_-614delinsCG | |
| NM_000127.3:c.-615_-614delinsCG MANE Select | NP_000118.2:n.-615_-614delinsCG |