Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28767687_28767748del , CM000676.2:g.28767687_28767748del | GRCh38 |
| NC_000014.8:g.29236893_29236954del , CM000676.1:g.29236893_29236954del | GRCh37 |
| NC_000014.7:g.28306644_28306705del | NCBI36 |
| NG_009367.1:g.5607_5668del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706482.1:c.408_469del | ENSP00000516406.1:p.Leu137GlyfsTer? | |
| ENST00000313071.7:c.408_469del MANE Select | ENSP00000339004.3:p.Leu137GlyfsTer? | |
| ENST00000313071.6:c.408_469del | ENSP00000339004.3:p.Leu137GlyfsTer? | |
| NM_005249.4:c.408_469del | NP_005240.3:p.Leu137GlyfsTer? | |
| NM_005249.5:c.408_469del MANE Select | NP_005240.3:p.Leu137GlyfsTer? |