HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780701_94780702delinsCT , CM000672.2:g.94780701_94780702delinsCT | GRCh38 |
NC_000010.10:g.96540458_96540459delinsCT , CM000672.1:g.96540458_96540459delinsCT | GRCh37 |
NC_000010.9:g.96530448_96530449delinsCT | NCBI36 |
NG_008384.2:g.22996_22997delinsCT | |
NG_008384.3:g.23021_23022delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.642+42_642+43delinsCT MANE Select | ENSP00000360372.3:n.642+42_642+43delinsCT... | |
ENST00000645461.1:n.1695+42_1695+43delinsCT | ||
ENST00000371321.7:c.642+42_642+43delinsCT | ENSP00000360372.3:n.642+42_642+43delinsCT... | |
ENST00000464755.1:c.1405+42_1405+43delinsCT | ENSP00000483243.1:n.1405+42_1405+43delins... | |
NM_000769.2:c.642+42_642+43delinsCT | NP_000760.1:n.642+42_642+43delinsCT | |
NM_000769.4:c.642+42_642+43delinsCT MANE Select | NP_000760.1:n.642+42_642+43delinsCT |