HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461600_122461602delinsGCT , CM000672.2:g.122461600_122461602delinsGCT | GRCh38 |
NC_000010.10:g.124221116_124221118delinsGCT , CM000672.1:g.124221116_124221118delinsGCT | GRCh37 |
NC_000010.9:g.124211106_124211108delinsGCT | NCBI36 |
NG_011554.1:g.5076_5078delinsGCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.-53_-51delinsGCT MANE Select | ENSP00000357980.3:n.-53_-51delinsGCT | |
ENST00000648167.1:c.154+2891_154+2893delinsGCT | ENSP00000498033.1:n.154+2891_154+2893delinsGCT | |
ENST00000368984.7:c.-53_-51delinsGCT | ENSP00000357980.3:n.-53_-51delinsGCT | |
NM_002775.4:c.-53_-51delinsGCT | NP_002766.1:n.-53_-51delinsGCT | |
NM_002775.5:c.-53_-51delinsGCT MANE Select | NP_002766.1:n.-53_-51delinsGCT |