Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.146340089_146340102del , CM000667.2:g.146340089_146340102del | GRCh38 |
| NC_000005.9:g.145719652_145719665del , CM000667.1:g.145719652_145719665del | GRCh37 |
| NC_000005.8:g.145699845_145699858del | NCBI36 |
| NG_011885.1:g.6066_6079del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646991.2:c.662_675del MANE Select | ENSP00000495718.1:p.Gly221GlufsTer? | |
| ENST00000230732.4:c.662_675del | ENSP00000230732.4:p.Gly221GlufsTer? | |
| NM_002700.2:c.662_675del | NP_002691.1:p.Gly221GlufsTer? | |
| NM_002700.3:c.662_675del MANE Select | NP_002691.1:p.Gly221GlufsTer? |