HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780379_94780382del , CM000672.2:g.94780379_94780382del | GRCh38 |
NC_000010.10:g.96540136_96540139del , CM000672.1:g.96540136_96540139del | GRCh37 |
NC_000010.9:g.96530126_96530129del | NCBI36 |
NG_008384.2:g.22674_22677del | |
NG_008384.3:g.22699_22702del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.482-120_482-117del MANE Select | ENSP00000360372.3:n.482-120_482-117del | |
ENST00000645461.1:n.1535-120_1535-117del | ||
ENST00000371321.7:c.482-120_482-117del | ENSP00000360372.3:n.482-120_482-117del | |
ENST00000464755.1:c.1245-120_1245-117del | ENSP00000483243.1:n.1245-120_1245-117del | |
NM_000769.2:c.482-120_482-117del | NP_000760.1:n.482-120_482-117del | |
NM_000769.4:c.482-120_482-117del MANE Select | NP_000760.1:n.482-120_482-117del |