HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115738491_115738492delinsAG , CM000663.2:g.115738491_115738492delinsAG | GRCh38 |
NC_000001.10:g.116281112_116281113delinsAG , CM000663.1:g.116281112_116281113delinsAG | GRCh37 |
NC_000001.9:g.116082635_116082636delinsAG | NCBI36 |
NG_008802.1:g.35314_35315delinsCT , LRG_404:g.35314_35315delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000488931.2:c.145-157_145-156delinsCT | ENSP00000518226.1:n.145-157_145-156delinsCT | |
ENST00000261448.6:c.421-157_421-156delinsCT MANE Select | ENSP00000261448.5:n.421-157_421-156delinsCT | |
ENST00000261448.5:c.421-157_421-156delinsCT | ENSP00000261448.5:n.421-157_421-156delinsCT | |
NM_001232.3:c.421-157_421-156delinsCT , LRG_404t1:c.421-157_421-156delinsCT | NP_001223.2:n.421-157_421-156delinsCT | |
NM_001232.4:c.421-157_421-156delinsCT MANE Select | NP_001223.2:n.421-157_421-156delinsCT |