HGVS | Genome Assembly |
---|---|
NC_000015.10:g.45480166_45480167delinsTA , CM000677.2:g.45480166_45480167delinsTA | GRCh38 |
NC_000015.9:g.45772364_45772365delinsTA , CM000677.1:g.45772364_45772365delinsTA | GRCh37 |
NC_000015.8:g.43559656_43559657delinsTA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261867.5:c.*4996_*4997delinsTA MANE Select | ENSP00000261867.3:n.*4996_*4997delinsTA | |
ENST00000261867.4:c.*4996_*4997delinsTA | ENSP00000261867.3:n.*4996_*4997delinsTA | |
NM_013309.5:c.*4996_*4997delinsTA | NP_037441.2:n.*4996_*4997delinsTA | |
NM_013309.6:c.*4996_*4997delinsTA MANE Select | NP_037441.2:n.*4996_*4997delinsTA |