Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.91107174_91107176delinsAAC , CM000674.2:g.91107174_91107176delinsAAC | GRCh38 |
| NC_000012.11:g.91500951_91500953delinsAAC , CM000674.1:g.91500951_91500953delinsAAC | GRCh37 |
| NC_000012.10:g.90025082_90025084delinsAAC | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266718.5:c.862+942_862+944delinsGTT MANE Select | ENSP00000266718.4:n.862+942_862+944delinsGTT | |
| ENST00000266718.4:c.862+942_862+944delinsGTT | ENSP00000266718.4:n.862+942_862+944delinsGTT | |
| ENST00000546642.1:n.612+942_612+944delinsGTT | ||
| ENST00000548071.1:n.255+942_255+944delinsGTT | ||
| NM_002345.3:c.862+942_862+944delinsGTT | NP_002336.1:n.862+942_862+944delinsGTT | |
| NM_002345.4:c.862+942_862+944delinsGTT MANE Select | NP_002336.1:n.862+942_862+944delinsGTT |