Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.72020956_72020957delinsAC , CM000674.2:g.72020956_72020957delinsAC | GRCh38 |
| NC_000012.11:g.72414736_72414737delinsAC , CM000674.1:g.72414736_72414737delinsAC | GRCh37 |
| NC_000012.10:g.70701003_70701004delinsAC | NCBI36 |
| NG_008279.1:g.87111_87112delinsAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333850.4:c.1069-1443_1069-1442delinsAC MANE Select | ENSP00000329093.3:n.1069-1443_1069-1442delinsAC | |
| ENST00000333850.3:c.1069-1443_1069-1442delinsAC | ENSP00000329093.3:n.1069-1443_1069-1442delinsAC | |
| NM_173353.3:c.1069-1443_1069-1442delinsAC | NP_775489.2:n.1069-1443_1069-1442delinsAC | |
| XM_011537899.1:c.475-1443_475-1442delinsAC | XP_011536201.1:n.475-1443_475-1442delinsAC | |
| NM_173353.4:c.1069-1443_1069-1442delinsAC MANE Select | NP_775489.2:n.1069-1443_1069-1442delinsAC |