Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21010261_21010264delinsCAAT , CM000664.2:g.21010261_21010264delinsCAAT | GRCh38 |
| NC_000002.11:g.21233133_21233136delinsCAAT , CM000664.1:g.21233133_21233136delinsCAAT | GRCh37 |
| NC_000002.10:g.21086638_21086641delinsCAAT | NCBI36 |
| NG_011793.1:g.38810_38813delinsATTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.6604_6607delinsATTG MANE Select | ENSP00000233242.1:p.Ile2202= | |
| ENST00000616098.4:c.6604_6607delinsATTG | ENSP00000477990.1:p.Ile2202= | |
| NM_000384.2:c.6604_6607delinsATTG | NP_000375.2:p.Ile2202= | |
| XM_011532809.1:c.5869+469_5869+472delinsATTG | XP_011531111.1:n.5869+469_5869+472delinsATTG | |
| NM_000384.3:c.6604_6607delinsATTG MANE Select | NP_000375.3:p.Ile2202= |