Linked Data
gnomAD v4:
5-111071729-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071729_111071730insA , CM000667.2:g.111071729_111071730insA | GRCh38 |
| NC_000005.9:g.110407427_110407428insA , CM000667.1:g.110407427_110407428insA | GRCh37 |
| NC_000005.8:g.110435326_110435327insA | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.-162_-161insA MANE Select | ENSP00000339804.3:n.-162_-161insA | |
| ENST00000344895.3:c.-162_-161insA | ENSP00000339804.3:n.-162_-161insA | |
| ENST00000420978.6:c.35-196_35-195insA | ENSP00000399099.2:n.35-196_35-195insA | |
| NM_033035.4:c.-162_-161insA | NP_149024.1:n.-162_-161insA | |
| NR_045089.1:n.1439-196_1439-195insA | ||
| NM_033035.5:c.-162_-161insA MANE Select | NP_149024.1:n.-162_-161insA | |
| NR_045089.2:n.1457-196_1457-195insA |