Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202377325_202377327delinsCCT , CM000664.2:g.202377325_202377327delinsCCT | GRCh38 |
| NC_000002.11:g.203242048_203242050delinsCCT , CM000664.1:g.203242048_203242050delinsCCT | GRCh37 |
| NC_000002.10:g.202950293_202950295delinsCCT | NCBI36 |
| NG_009363.1:g.5999_6001delinsCCT , LRG_712:g.5999_6001delinsCCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.-150_-148delinsCCT MANE Select | ENSP00000363708.4:n.-150_-148delinsCCT | |
| ENST00000374580.8:c.-150_-148delinsCCT | ENSP00000363708.4:n.-150_-148delinsCCT | |
| NM_001204.6:c.-150_-148delinsCCT , LRG_712t1:c.-150_-148delinsCCT | NP_001195.2:n.-150_-148delinsCCT | |
| XM_011511687.1:c.-150_-148delinsCCT | XP_011509989.1:n.-150_-148delinsCCT | |
| XM_011511688.1:c.-150_-148delinsCCT | XP_011509990.1:n.-150_-148delinsCCT | |
| NM_001204.7:c.-150_-148delinsCCT MANE Select | NP_001195.2:n.-150_-148delinsCCT |