Linked Data
gnomAD v4:
5-111071834-T-TCCC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071834_111071835insCCC , CM000667.2:g.111071834_111071835insCCC | GRCh38 |
| NC_000005.9:g.110407532_110407533insCCC , CM000667.1:g.110407532_110407533insCCC | GRCh37 |
| NC_000005.8:g.110435431_110435432insCCC | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.-57_-56insCCC MANE Select | ENSP00000339804.3:n.-57_-56insCCC | |
| ENST00000344895.3:c.-57_-56insCCC | ENSP00000339804.3:n.-57_-56insCCC | |
| ENST00000420978.6:c.35-91_35-90insCCC | ENSP00000399099.2:n.35-91_35-90insCCC | |
| NM_033035.4:c.-57_-56insCCC | NP_149024.1:n.-57_-56insCCC | |
| NR_045089.1:n.1439-91_1439-90insCCC | ||
| NM_033035.5:c.-57_-56insCCC MANE Select | NP_149024.1:n.-57_-56insCCC | |
| NR_045089.2:n.1457-91_1457-90insCCC |