Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658452_10658453insAA , CM000682.2:g.10658452_10658453insAA | GRCh38 |
| NC_000020.10:g.10639100_10639101insAA , CM000682.1:g.10639100_10639101insAA | GRCh37 |
| NC_000020.9:g.10587100_10587101insAA | NCBI36 |
| NG_007496.1:g.20595_20596insTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.694+16_694+17insTT MANE Select | ENSP00000254958.4:n.694+16_694+17insTT | |
| ENST00000254958.9:c.694+16_694+17insTT | ENSP00000254958.4:n.694+16_694+17insTT | |
| ENST00000423891.6:n.560+16_560+17insTT | ||
| NM_000214.2:c.694+16_694+17insTT | NP_000205.1:n.694+16_694+17insTT | |
| NM_000214.3:c.694+16_694+17insTT MANE Select | NP_000205.1:n.694+16_694+17insTT |