Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226709_5226714del , CM000673.2:g.5226709_5226714del | GRCh38 |
| NC_000011.9:g.5247939_5247944del , CM000673.1:g.5247939_5247944del | GRCh37 |
| NC_000011.8:g.5204515_5204520del | NCBI36 |
| NG_000007.3:g.70906_70911del | |
| NG_059281.1:g.5362_5367del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.182_187del | ENSP00000494175.1:p.Val61_Lys62del | |
| ENST00000335295.4:c.182_187del MANE Select | ENSP00000333994.3:p.Val61_Lys62del | |
| ENST00000380315.2:c.182_187del | ENSP00000369671.2:p.Val61_Lys62del | |
| ENST00000475226.1:n.114_119del | ||
| ENST00000485743.1:n.233_238del | ||
| ENST00000633227.1:c.166_*3del | ENSP00000488004.1:n.[c.166_*3del;Ter56LeuextTer27] | |
| NM_000518.4:c.182_187del | NP_000509.1:p.Val61_Lys62del | |
| NM_000518.5:c.182_187del MANE Select | NP_000509.1:p.Val61_Lys62del |