HGVS | Genome Assembly |
---|---|
NC_000016.10:g.23211256_23211270delinsGCCTGCCTTCAGGAA , CM000678.2:g.23211256_23211270delinsGCCTGCCTTCAGGAA | GRCh38 |
NC_000016.9:g.23222577_23222591delinsGCCTGCCTTCAGGAA , CM000678.1:g.23222577_23222591delinsGCCTGCCTTCAGGAA | GRCh37 |
NC_000016.8:g.23130078_23130092delinsGCCTGCCTTCAGGAA | NCBI36 |
NG_011909.1:g.33538_33552delinsGCCTGCCTTCAGGAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000300061.3:c.1177-778_1177-764delinsGCCTGCCTTCAGGAA MANE Select | ENSP00000300061.2:n.1177-778_1177-764delinsGCCTGCCTTCAGGAA | |
ENST00000300061.2:c.1177-778_1177-764delinsGCCTGCCTTCAGGAA | ENSP00000300061.2:n.1177-778_1177-764delinsGCCTGCCTTCAGGAA | |
NM_001039.3:c.1177-778_1177-764delinsGCCTGCCTTCAGGAA | NP_001030.2:n.1177-778_1177-764delinsGCCTGCCTTCAGGAA | |
NM_001039.4:c.1177-778_1177-764delinsGCCTGCCTTCAGGAA MANE Select | NP_001030.2:n.1177-778_1177-764delinsGCCTGCCTTCAGGAA |