Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.111071788_111071789del , CM000667.2:g.111071788_111071789del | GRCh38 |
| NC_000005.9:g.110407486_110407487del , CM000667.1:g.110407486_110407487del | GRCh37 |
| NC_000005.8:g.110435385_110435386del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344895.4:c.-103_-102del MANE Select | ENSP00000339804.3:n.-103_-102del | |
| ENST00000344895.3:c.-103_-102del | ENSP00000339804.3:n.-103_-102del | |
| ENST00000420978.6:c.35-137_35-136del | ENSP00000399099.2:n.35-137_35-136del | |
| NM_033035.4:c.-103_-102del | NP_149024.1:n.-103_-102del | |
| NR_045089.1:n.1439-137_1439-136del | ||
| NM_033035.5:c.-103_-102del MANE Select | NP_149024.1:n.-103_-102del | |
| NR_045089.2:n.1457-137_1457-136del |