HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122461586_122461587insCTG , CM000672.2:g.122461586_122461587insCTG | GRCh38 |
NC_000010.10:g.124221102_124221103insCTG , CM000672.1:g.124221102_124221103insCTG | GRCh37 |
NC_000010.9:g.124211092_124211093insCTG | NCBI36 |
NG_011554.1:g.5062_5063insCTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368984.8:c.-67_-66insCTG MANE Select | ENSP00000357980.3:n.-67_-66insCTG | |
ENST00000648167.1:c.154+2877_154+2878insCTG | ENSP00000498033.1:n.154+2877_154+2878insCTG | |
ENST00000368984.7:c.-67_-66insCTG | ENSP00000357980.3:n.-67_-66insCTG | |
NM_002775.4:c.-67_-66insCTG | NP_002766.1:n.-67_-66insCTG | |
NM_002775.5:c.-67_-66insCTG MANE Select | NP_002766.1:n.-67_-66insCTG |