HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115738473_115738474delinsTC , CM000663.2:g.115738473_115738474delinsTC | GRCh38 |
NC_000001.10:g.116281094_116281095delinsTC , CM000663.1:g.116281094_116281095delinsTC | GRCh37 |
NC_000001.9:g.116082617_116082618delinsTC | NCBI36 |
NG_008802.1:g.35332_35333delinsGA , LRG_404:g.35332_35333delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000488931.2:c.145-139_145-138delinsGA | ENSP00000518226.1:n.145-139_145-138delinsGA | |
ENST00000261448.6:c.421-139_421-138delinsGA MANE Select | ENSP00000261448.5:n.421-139_421-138delinsGA | |
ENST00000261448.5:c.421-139_421-138delinsGA | ENSP00000261448.5:n.421-139_421-138delinsGA | |
NM_001232.3:c.421-139_421-138delinsGA , LRG_404t1:c.421-139_421-138delinsGA | NP_001223.2:n.421-139_421-138delinsGA | |
NM_001232.4:c.421-139_421-138delinsGA MANE Select | NP_001223.2:n.421-139_421-138delinsGA |