Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10643983_10643984insA , CM000682.2:g.10643983_10643984insA | GRCh38 |
| NC_000020.10:g.10624631_10624632insA , CM000682.1:g.10624631_10624632insA | GRCh37 |
| NC_000020.9:g.10572631_10572632insA | NCBI36 |
| NG_007496.1:g.35063_35064insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.2373-121_2373-120insT MANE Select | ENSP00000254958.4:n.2373-121_2373-120insT | |
| ENST00000617965.2:n.2962-121_2962-120insT | ||
| ENST00000254958.9:c.2373-121_2373-120insT | ENSP00000254958.4:n.2373-121_2373-120insT | |
| ENST00000423891.6:n.2239-121_2239-120insT | ||
| NM_000214.2:c.2373-121_2373-120insT | NP_000205.1:n.2373-121_2373-120insT | |
| NM_000214.3:c.2373-121_2373-120insT MANE Select | NP_000205.1:n.2373-121_2373-120insT |