Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226758_5226766del , CM000673.2:g.5226758_5226766del | GRCh38 |
| NC_000011.9:g.5247988_5247996del , CM000673.1:g.5247988_5247996del | GRCh37 |
| NC_000011.8:g.5204564_5204572del | NCBI36 |
| NG_000007.3:g.70855_70863del | |
| NG_059281.1:g.5311_5319del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647020.1:c.131_139del | ENSP00000494175.1:p.Glu44_Phe46del | |
| ENST00000335295.4:c.131_139del MANE Select | ENSP00000333994.3:p.Glu44_Phe46del | |
| ENST00000380315.2:c.131_139del | ENSP00000369671.2:p.Glu44_Phe46del | |
| ENST00000475226.1:n.63_71del | ||
| ENST00000485743.1:n.182_190del | ||
| ENST00000633227.1:c.115_123del | ENSP00000488004.1:p.Ser39_Leu41del | |
| NM_000518.4:c.131_139del | NP_000509.1:p.Glu44_Phe46del | |
| NM_000518.5:c.131_139del MANE Select | NP_000509.1:p.Glu44_Phe46del |