Linked Data
gnomAD v4:
5-111071724-T-TC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071726dup , CM000667.2:g.111071726dup | GRCh38 |
| NC_000005.9:g.110407424dup , CM000667.1:g.110407424dup | GRCh37 |
| NC_000005.8:g.110435323dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.-165dup MANE Select | ENSP00000339804.3:n.-165dup | |
| ENST00000344895.3:c.-165dup | ENSP00000339804.3:n.-165dup | |
| ENST00000420978.6:c.35-199dup | ENSP00000399099.2:n.35-199dup | |
| NM_033035.4:c.-165dup | NP_149024.1:n.-165dup | |
| NR_045089.1:n.1439-199dup | ||
| NM_033035.5:c.-165dup MANE Select | NP_149024.1:n.-165dup | |
| NR_045089.2:n.1457-199dup |