HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94853027_94853028delinsTC , CM000672.2:g.94853027_94853028delinsTC | GRCh38 |
NC_000010.10:g.96612784_96612785delinsTC , CM000672.1:g.96612784_96612785delinsTC | GRCh37 |
NC_000010.9:g.96602774_96602775delinsTC | NCBI36 |
NG_008384.2:g.95322_95323delinsTC | |
NG_008384.3:g.95347_95348delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.*113_*114delinsTC MANE Select | ENSP00000360372.3:n.*113_*114delinsTC | |
ENST00000645461.1:n.2497_2498delinsTC | ||
ENST00000371321.7:c.*113_*114delinsTC | ENSP00000360372.3:n.*113_*114delinsTC | |
ENST00000464755.1:c.2349_2350delinsTC | ENSP00000483243.1:n.2349_2350delinsTC | |
NM_000769.2:c.*113_*114delinsTC | NP_000760.1:n.*113_*114delinsTC | |
NM_000769.4:c.*113_*114delinsTC MANE Select | NP_000760.1:n.*113_*114delinsTC |