Linked Data
gnomAD v4:
14-74259814-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.74259814_74259815insA , CM000676.2:g.74259814_74259815insA | GRCh38 |
| NC_000014.8:g.74726517_74726518insA , CM000676.1:g.74726517_74726518insA | GRCh37 |
| NC_000014.7:g.73796270_73796271insA | NCBI36 |
| NG_013092.1:g.25343_25344insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261980.3:c.760+32_760+33insA MANE Select | ENSP00000261980.2:n.760+32_760+33insA | |
| ENST00000261980.2:c.760+32_760+33insA | ENSP00000261980.2:n.760+32_760+33insA | |
| NM_182894.2:c.760+32_760+33insA | NP_878314.1:n.760+32_760+33insA | |
| XM_011536719.1:c.760+32_760+33insA | XP_011535021.1:n.760+32_760+33insA | |
| NM_182894.3:c.760+32_760+33insA MANE Select | NP_878314.1:n.760+32_760+33insA |