Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.34256001_34256002delinsAT , CM000679.2:g.34256001_34256002delinsAT | GRCh38 |
| NC_000017.10:g.32583020_32583021delinsAT , CM000679.1:g.32583020_32583021delinsAT | GRCh37 |
| NC_000017.9:g.29607133_29607134delinsAT | NCBI36 |
| NG_012123.1:g.5725_5726delinsAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580907.6:c.77-221_77-220delinsAT | ENSP00000462156.1:n.77-221_77-220delinsAT | |
| ENST00000624362.2:n.717_718delinsAT | ||
| ENST00000225831.4:c.77-221_77-220delinsAT MANE Select | ENSP00000225831.4:n.77-221_77-220delinsAT | |
| ENST00000580907.5:c.77-221_77-220delinsAT | ENSP00000462156.1:n.77-221_77-220delinsAT | |
| ENST00000624362.1:n.784_785delinsAT | ||
| NM_002982.3:c.77-221_77-220delinsAT | NP_002973.1:n.77-221_77-220delinsAT | |
| NM_002982.4:c.77-221_77-220delinsAT MANE Select | NP_002973.1:n.77-221_77-220delinsAT |