Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215867247_215867248insAGA , CM000663.2:g.215867247_215867248insAGA | GRCh38 |
| NC_000001.10:g.216040589_216040590insAGA , CM000663.1:g.216040589_216040590insAGA | GRCh37 |
| NC_000001.9:g.214107212_214107213insAGA | NCBI36 |
| NG_009497.1:g.561149_561150insTCT | |
| NG_009497.2:g.561201_561202insTCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.8682-78_8682-77insTCT MANE Select | ENSP00000305941.3:n.8682-78_8682-77insTCT | |
| ENST00000674083.1:c.8682-78_8682-77insTCT | ENSP00000501296.1:n.8682-78_8682-77insTCT | |
| ENST00000307340.7:c.8682-78_8682-77insTCT | ENSP00000305941.3:n.8682-78_8682-77insTCT | |
| NM_206933.2:c.8682-78_8682-77insTCT | NP_996816.2:n.8682-78_8682-77insTCT | |
| NM_206933.3:c.8682-78_8682-77insTCT | NP_996816.2:n.8682-78_8682-77insTCT | |
| NM_206933.4:c.8682-78_8682-77insTCT MANE Select | NP_996816.3:n.8682-78_8682-77insTCT |