HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584067_41584071delinsCTCTT , CM000679.2:g.41584067_41584071delinsCTCTT | GRCh38 |
NC_000017.10:g.39740319_39740323delinsCTCTT , CM000679.1:g.39740319_39740323delinsCTCTT | GRCh37 |
NC_000017.9:g.36993845_36993849delinsCTCTT | NCBI36 |
NG_008624.1:g.7825_7829delinsAAGAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.766-150_766-146delinsAAGAG MANE Select | ENSP00000167586.6:n.766-150_766-146delinsAAGAG | |
ENST00000167586.6:c.766-150_766-146delinsAAGAG | ENSP00000167586.6:n.766-150_766-146delinsAAGAG | |
ENST00000476662.1:n.216-150_216-146delinsAAGAG | ||
NM_000526.4:c.766-150_766-146delinsAAGAG | NP_000517.2:n.766-150_766-146delinsAAGAG | |
NM_000526.5:c.766-150_766-146delinsAAGAG MANE Select | NP_000517.3:n.766-150_766-146delinsAAGAG |