HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215799176_215799177insAG , CM000663.2:g.215799176_215799177insAG | GRCh38 |
NC_000001.10:g.215972518_215972519insAG , CM000663.1:g.215972518_215972519insAG | GRCh37 |
NC_000001.9:g.214039141_214039142insAG | NCBI36 |
NG_009497.1:g.629220_629221insCT | |
NG_009497.2:g.629272_629273insCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.9740-52_9740-51insCT MANE Select | ENSP00000305941.3:n.9740-52_9740-51insCT | |
ENST00000674083.1:c.9740-52_9740-51insCT | ENSP00000501296.1:n.9740-52_9740-51insCT | |
ENST00000307340.7:c.9740-52_9740-51insCT | ENSP00000305941.3:n.9740-52_9740-51insCT | |
NM_206933.2:c.9740-52_9740-51insCT | NP_996816.2:n.9740-52_9740-51insCT | |
NM_206933.3:c.9740-52_9740-51insCT | NP_996816.2:n.9740-52_9740-51insCT | |
NM_206933.4:c.9740-52_9740-51insCT MANE Select | NP_996816.3:n.9740-52_9740-51insCT |