HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215675662_215675663insA , CM000663.2:g.215675662_215675663insA | GRCh38 |
NC_000001.10:g.215849004_215849005insA , CM000663.1:g.215849004_215849005insA | GRCh37 |
NC_000001.9:g.213915627_213915628insA | NCBI36 |
NG_009497.1:g.752734_752735insT | |
NG_009497.2:g.752786_752787insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.12295-47_12295-46insT MANE Select | ENSP00000305941.3:n.12295-47_12295-46insT | |
ENST00000674083.1:c.12295-47_12295-46insT | ENSP00000501296.1:n.12295-47_12295-46insT | |
ENST00000307340.7:c.12295-47_12295-46insT | ENSP00000305941.3:n.12295-47_12295-46insT | |
NM_206933.2:c.12295-47_12295-46insT | NP_996816.2:n.12295-47_12295-46insT | |
NM_206933.3:c.12295-47_12295-46insT | NP_996816.2:n.12295-47_12295-46insT | |
NM_206933.4:c.12295-47_12295-46insT MANE Select | NP_996816.3:n.12295-47_12295-46insT |