HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65246339_65246340insT , CM000674.2:g.65246339_65246340insT | GRCh38 |
NC_000012.11:g.65640119_65640120insT , CM000674.1:g.65640119_65640120insT | GRCh37 |
NC_000012.10:g.63926386_63926387insT | NCBI36 |
NG_016210.1:g.81769_81770insT | |
NG_016210.2:g.81769_81770insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.*14_*15insT MANE Select | ENSP00000308369.2:n.*14_*15insT | |
ENST00000308330.2:c.*14_*15insT | ENSP00000308369.2:n.*14_*15insT | |
ENST00000539442.1:n.732_733insT | ||
ENST00000545026.1:n.568_569insT | ||
NM_001167614.1:c.*14_*15insT | NP_001161086.1:n.*14_*15insT | |
NM_014319.4:c.*14_*15insT | NP_055134.2:n.*14_*15insT | |
NM_014319.5:c.*14_*15insT MANE Select | NP_055134.2:n.*14_*15insT | |
NM_001167614.2:c.*14_*15insT | NP_001161086.1:n.*14_*15insT |