HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584070_41584071insCTCTTT , CM000679.2:g.41584070_41584071insCTCTTT | GRCh38 |
NC_000017.10:g.39740322_39740323insCTCTTT , CM000679.1:g.39740322_39740323insCTCTTT | GRCh37 |
NC_000017.9:g.36993848_36993849insCTCTTT | NCBI36 |
NG_008624.1:g.7826_7827insAAGAGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.766-149_766-148insAAGAGA MANE Select | ENSP00000167586.6:n.766-149_766-148insAAGAGA | |
ENST00000167586.6:c.766-149_766-148insAAGAGA | ENSP00000167586.6:n.766-149_766-148insAAGAGA | |
ENST00000476662.1:n.216-149_216-148insAAGAGA | ||
NM_000526.4:c.766-149_766-148insAAGAGA | NP_000517.2:n.766-149_766-148insAAGAGA | |
NM_000526.5:c.766-149_766-148insAAGAGA MANE Select | NP_000517.3:n.766-149_766-148insAAGAGA |