HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215799182_215799183insCAT , CM000663.2:g.215799182_215799183insCAT | GRCh38 |
NC_000001.10:g.215972524_215972525insCAT , CM000663.1:g.215972524_215972525insCAT | GRCh37 |
NC_000001.9:g.214039147_214039148insCAT | NCBI36 |
NG_009497.1:g.629214_629215insATG | |
NG_009497.2:g.629266_629267insATG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.9740-58_9740-57insATG MANE Select | ENSP00000305941.3:n.9740-58_9740-57insATG | |
ENST00000674083.1:c.9740-58_9740-57insATG | ENSP00000501296.1:n.9740-58_9740-57insATG | |
ENST00000307340.7:c.9740-58_9740-57insATG | ENSP00000305941.3:n.9740-58_9740-57insATG | |
NM_206933.2:c.9740-58_9740-57insATG | NP_996816.2:n.9740-58_9740-57insATG | |
NM_206933.3:c.9740-58_9740-57insATG | NP_996816.2:n.9740-58_9740-57insATG | |
NM_206933.4:c.9740-58_9740-57insATG MANE Select | NP_996816.3:n.9740-58_9740-57insATG |