Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39665388_39665396del , CM000679.2:g.39665388_39665396del | GRCh38 |
| NC_000017.10:g.37821641_37821649del , CM000679.1:g.37821641_37821649del | GRCh37 |
| NC_000017.9:g.35075167_35075175del | NCBI36 |
| NG_008892.1:g.5043_5051del , LRG_210:g.5043_5051del | |
| NG_042278.1:g.2408_2416del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309889.3:c.29_37del MANE Select | ENSP00000312624.2:p.Val10_Glu12del | |
| ENST00000309889.2:c.29_37del | ENSP00000312624.2:p.Val10_Glu12del | |
| ENST00000578283.1:c.29_37del | ENSP00000462787.1:p.Val10_Glu12del | |
| NM_003673.3:c.29_37del , LRG_210t1:c.29_37del | NP_003664.1:p.Val10_Glu12del | |
| NM_003673.4:c.29_37del MANE Select | NP_003664.1:p.Val10_Glu12del |