HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41612696_41612697delinsAG , CM000679.2:g.41612696_41612697delinsAG | GRCh38 |
NC_000017.10:g.39768948_39768949delinsAG , CM000679.1:g.39768948_39768949delinsAG | GRCh37 |
NC_000017.9:g.37022474_37022475delinsAG | NCBI36 |
NG_008301.1:g.5131_5132delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301653.9:c.-9_-8delinsCT MANE Select | ENSP00000301653.3:n.-9_-8delinsCT | |
ENST00000301653.8:c.-9_-8delinsCT | ENSP00000301653.3:n.-9_-8delinsCT | |
ENST00000588319.1:n.69_70delinsCT | ||
ENST00000590990.1:c.-9_-8delinsCT | ENSP00000467105.1:n.-9_-8delinsCT | |
ENST00000593067.1:c.-313+93_-313+94delinsCT | ENSP00000467124.1:n.-313+93_-313+94delinsCT | |
NM_005557.3:c.-9_-8delinsCT | NP_005548.2:n.-9_-8delinsCT | |
NM_005557.4:c.-9_-8delinsCT MANE Select | NP_005548.2:n.-9_-8delinsCT |