HGVS | Genome Assembly |
---|---|
NC_000006.12:g.39215707_39215709delinsATG , CM000668.2:g.39215707_39215709delinsATG | GRCh38 |
NC_000006.11:g.39183483_39183485delinsATG , CM000668.1:g.39183483_39183485delinsATG | GRCh37 |
NC_000006.10:g.39291461_39291463delinsATG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000359534.4:c.186+13217_186+13219delinsCAT MANE Select | ENSP00000352527.3:n.186+13217_186+13219delinsCAT | |
ENST00000359534.3:c.186+13217_186+13219delinsCAT | ENSP00000352527.3:n.186+13217_186+13219delinsCAT | |
NM_003740.3:c.186+13217_186+13219delinsCAT | NP_003731.1:n.186+13217_186+13219delinsCAT | |
XM_005249456.1:c.186+13217_186+13219delinsCAT | XP_005249513.1:n.186+13217_186+13219delinsCAT | |
NM_003740.4:c.186+13217_186+13219delinsCAT MANE Select | NP_003731.1:n.186+13217_186+13219delinsCAT |