HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24146053_24146054insCCAAATC , CM000668.2:g.24146053_24146054insCCAAATC | GRCh38 |
NC_000006.11:g.24146281_24146282insCCAAATC , CM000668.1:g.24146281_24146282insCCAAATC | GRCh37 |
NC_000006.10:g.24254260_24254261insCCAAATC | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378491.9:c.*107_*108insCCAAATC MANE Select | ENSP00000367752.4:n.*107_*108insCCAAATC | |
ENST00000378478.5:c.*107_*108insCCAAATC | ENSP00000367739.2:n.*107_*108insCCAAATC | |
ENST00000378491.8:c.*107_*108insCCAAATC | ENSP00000367752.4:n.*107_*108insCCAAATC | |
ENST00000468195.2:n.257-8718_257-8717insCCAAATC | ||
NM_080723.4:c.*107_*108insCCAAATC | NP_542454.3:n.*107_*108insCCAAATC | |
NM_080723.5:c.*107_*108insCCAAATC MANE Select | NP_542454.3:n.*107_*108insCCAAATC |