Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.141973218_141973219insCCCAACACA , CM000669.2:g.141973218_141973219insCCCAACACA | GRCh38 |
| NC_000007.13:g.141673018_141673019insCCCAACACA , CM000669.1:g.141673018_141673019insCCCAACACA | GRCh37 |
| NC_000007.12:g.141319487_141319488insCCCAACACA | NCBI36 |
| NG_016141.1:g.5561_5562insGGGTGTGTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465654.5:c.-3+27221_-3+27222insCCCAACACA (MGAM) | ENSP00000419372.1:n.-3+27221_-3+27222insCCCAACACA | |
| ENST00000547270.1:c.477_478insGGGTGTGTT (TAS2R38) MANE Select | ENSP00000448219.1:p.Val159_Trp160insGlyCysVal | |
| NM_176817.4:c.477_478insGGGTGTGTT (TAS2R38) | NP_789787.4:p.Val159_Trp160insGlyCysVal | |
| XM_011515783.1:c.*25-13178_*25-13177insCCCAACACA (OR9A4) | XP_011514085.1:n.*25-13178_*25-13177insCCCAACACA | |
| NM_176817.5:c.477_478insGGGTGTGTT (TAS2R38) MANE Select | NP_789787.5:p.Val159_Trp160insGlyCysVal |