Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35851595_35851596del , CM000681.2:g.35851595_35851596del | GRCh38 |
| NC_000019.9:g.36342497_36342498del , CM000681.1:g.36342497_36342498del | GRCh37 |
| NC_000019.8:g.41034337_41034338del | NCBI36 |
| NG_013356.2:g.22695_22696del , LRG_693:g.22695_22696del | |
| NG_051206.1:g.4961_4962del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004646.4:c.138_139del MANE Select | NP_004637.1:p.Ala47LeufsTer? |
| ENST00000378910.10:c.138_139del MANE Select | ENSP00000368190.4:p.Ala47LeufsTer? |
| NM_004646.3:c.138_139del , LRG_693t1:c.138_139del | NP_004637.1:p.Ala47LeufsTer? |
| ENST00000353632.6:c.138_139del | ENSP00000343634.5:p.Ala47LeufsTer? |
| ENST00000378910.9:c.138_139del | ENSP00000368190.4:p.Ala47LeufsTer? |