HGVS | Genome Assembly |
---|---|
NC_000011.10:g.102842593_102842594delinsAT , CM000673.2:g.102842593_102842594delinsAT | GRCh38 |
NC_000011.9:g.102713324_102713325delinsAT , CM000673.1:g.102713324_102713325delinsAT | GRCh37 |
NC_000011.8:g.102218534_102218535delinsAT | NCBI36 |
NG_012100.1:g.6018_6019delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299855.10:c.351-15_351-14delinsAT MANE Select | ENSP00000299855.5:n.351-15_351-14delinsAT | |
ENST00000299855.9:c.351-15_351-14delinsAT | ENSP00000299855.5:n.351-15_351-14delinsAT | |
ENST00000524478.1:c.*193-15_*193-14delinsAT | ENSP00000435255.1:n.*193-15_*193-14delinsAT | |
NM_002422.3:c.351-15_351-14delinsAT | NP_002413.1:n.351-15_351-14delinsAT | |
NM_002422.4:c.351-15_351-14delinsAT | NP_002413.1:n.351-15_351-14delinsAT | |
NM_002422.5:c.351-15_351-14delinsAT MANE Select | NP_002413.1:n.351-15_351-14delinsAT |