Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94401645_94401646delinsCA , CM000669.2:g.94401645_94401646delinsCA | GRCh38 |
| NC_000007.13:g.94030957_94030958delinsCA , CM000669.1:g.94030957_94030958delinsCA | GRCh37 |
| NC_000007.12:g.93868893_93868894delinsCA | NCBI36 |
| NG_007405.1:g.12085_12086delinsCA , LRG_2:g.12085_12086delinsCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.279+25_279+26delinsCA MANE Select | ENSP00000297268.6:n.279+25_279+26delinsCA | |
| ENST00000297268.10:c.279+25_279+26delinsCA | ENSP00000297268.6:n.279+25_279+26delinsCA | |
| ENST00000620463.1:c.273+25_273+26delinsCA | ENSP00000477719.1:n.273+25_273+26delinsCA | |
| NM_000089.3:c.279+25_279+26delinsCA , LRG_2t1:c.279+25_279+26delinsCA | NP_000080.2:n.279+25_279+26delinsCA | |
| NM_000089.4:c.279+25_279+26delinsCA MANE Select | NP_000080.2:n.279+25_279+26delinsCA |