HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213378_1213379insCCA , CM000667.2:g.1213378_1213379insCCA | GRCh38 |
NC_000005.9:g.1213493_1213494insCCA , CM000667.1:g.1213493_1213494insCCA | GRCh37 |
NC_000005.8:g.1266493_1266494insCCA | NCBI36 |
NG_008282.1:g.16784_16785insCCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.664-85_664-84insCCA MANE Select | ENSP00000305302.10:n.664-85_664-84insCCA | |
ENST00000304460.10:c.664-85_664-84insCCA | ENSP00000305302.10:n.664-85_664-84insCCA | |
ENST00000515652.5:c.572-85_572-84insCCA | ENSP00000425701.1:n.572-85_572-84insCCA | |
NM_001003841.2:c.664-85_664-84insCCA | NP_001003841.1:n.664-85_664-84insCCA | |
NM_001003841.3:c.664-85_664-84insCCA MANE Select | NP_001003841.1:n.664-85_664-84insCCA |