Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665562_39665563delinsTG , CM000679.2:g.39665562_39665563delinsTG | GRCh38 |
| NC_000017.10:g.37821815_37821816delinsTG , CM000679.1:g.37821815_37821816delinsTG | GRCh37 |
| NC_000017.9:g.35075341_35075342delinsTG | NCBI36 |
| NG_008892.1:g.5217_5218delinsTG , LRG_210:g.5217_5218delinsTG | |
| NG_042278.1:g.2582_2583delinsTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.110+93_110+94delinsTG MANE Select | ENSP00000312624.2:n.110+93_110+94delinsTG | |
| ENST00000309889.2:c.110+93_110+94delinsTG | ENSP00000312624.2:n.110+93_110+94delinsTG | |
| ENST00000578283.1:c.110+93_110+94delinsTG | ENSP00000462787.1:n.110+93_110+94delinsTG | |
| NM_003673.3:c.110+93_110+94delinsTG , LRG_210t1:c.110+93_110+94delinsTG | NP_003664.1:n.110+93_110+94delinsTG | |
| NM_003673.4:c.110+93_110+94delinsTG MANE Select | NP_003664.1:n.110+93_110+94delinsTG |