HGVS | Genome Assembly |
---|---|
NC_000001.11:g.216070410_216070411insG , CM000663.2:g.216070410_216070411insG | GRCh38 |
NC_000001.10:g.216243752_216243753insG , CM000663.1:g.216243752_216243753insG | GRCh37 |
NC_000001.9:g.214310375_214310376insG | NCBI36 |
NG_009497.1:g.357986_357987insC | |
NG_009497.2:g.358038_358039insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.5858-119_5858-118insC MANE Select | ENSP00000305941.3:n.5858-119_5858-118insC | |
ENST00000674083.1:c.5858-119_5858-118insC | ENSP00000501296.1:n.5858-119_5858-118insC | |
ENST00000307340.7:c.5858-119_5858-118insC | ENSP00000305941.3:n.5858-119_5858-118insC | |
NM_206933.2:c.5858-119_5858-118insC | NP_996816.2:n.5858-119_5858-118insC | |
NM_206933.3:c.5858-119_5858-118insC | NP_996816.2:n.5858-119_5858-118insC | |
NM_206933.4:c.5858-119_5858-118insC MANE Select | NP_996816.3:n.5858-119_5858-118insC |