Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150992685_150992689delinsCTTGT , CM000669.2:g.150992685_150992689delinsCTTGT | GRCh38 |
| NC_000007.13:g.150689773_150689777delinsCTTGT , CM000669.1:g.150689773_150689777delinsCTTGT | GRCh37 |
| NC_000007.12:g.150320706_150320710delinsCTTGT | NCBI36 |
| NG_011992.1:g.6627_6631delinsCTTGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297494.8:c.-51-1068_-51-1064delinsCTTGT MANE Select | ENSP00000297494.3:n.-51-1068_-51-1064delinsCTTGT | |
| ENST00000297494.7:c.-51-1068_-51-1064delinsCTTGT | ENSP00000297494.3:n.-51-1068_-51-1064delinsCTTGT | |
| ENST00000461406.5:c.-149+1385_-149+1389delinsCTTGT | ENSP00000417143.1:n.-149+1385_-149+1389delinsCTTGT | |
| NM_000603.4:c.-51-1068_-51-1064delinsCTTGT | NP_000594.2:n.-51-1068_-51-1064delinsCTTGT | |
| NM_000603.5:c.-51-1068_-51-1064delinsCTTGT MANE Select | NP_000594.2:n.-51-1068_-51-1064delinsCTTGT |