HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122472380_122472381insCTA , CM000672.2:g.122472380_122472381insCTA | GRCh38 |
NC_000010.10:g.124231896_124231897insCTA , CM000672.1:g.124231896_124231897insCTA | GRCh37 |
NC_000010.9:g.124221886_124221887insCTA | NCBI36 |
NG_011554.1:g.15856_15857insCTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.472+10256_472+10257insCTA MANE Select | ENSP00000357980.3:n.472+10256_472+10257insCTA | |
ENST00000648167.1:c.154+13671_154+13672insCTA | ENSP00000498033.1:n.154+13671_154+13672insCTA | |
ENST00000368984.7:c.472+10256_472+10257insCTA | ENSP00000357980.3:n.472+10256_472+10257insCTA | |
NM_002775.4:c.472+10256_472+10257insCTA | NP_002766.1:n.472+10256_472+10257insCTA | |
NM_002775.5:c.472+10256_472+10257insCTA MANE Select | NP_002766.1:n.472+10256_472+10257insCTA |