HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94775815_94775882del , CM000672.2:g.94775815_94775882del | GRCh38 |
NC_000010.10:g.96535572_96535639del , CM000672.1:g.96535572_96535639del | GRCh37 |
NC_000010.9:g.96525562_96525629del | NCBI36 |
NG_008384.2:g.18110_18177del | |
NG_008384.3:g.18135_18202del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.481+276_481+343del MANE Select | ENSP00000360372.3:n.481+276_481+343del | |
ENST00000645461.1:n.1534+276_1534+343del | ||
ENST00000371321.7:c.481+276_481+343del | ENSP00000360372.3:n.481+276_481+343del | |
ENST00000464755.1:c.1244+276_1244+343del | ENSP00000483243.1:n.1244+276_1244+343del | |
ENST00000480405.2:c.*268_*335del | ENSP00000483847.1:n.*268_*335del | |
NM_000769.2:c.481+276_481+343del | NP_000760.1:n.481+276_481+343del | |
NM_000769.4:c.481+276_481+343del MANE Select | NP_000760.1:n.481+276_481+343del |