HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19954099_19954102delinsCCTG , CM000670.2:g.19954099_19954102delinsCCTG | GRCh38 |
NC_000008.10:g.19811610_19811613delinsCCTG , CM000670.1:g.19811610_19811613delinsCCTG | GRCh37 |
NC_000008.9:g.19855890_19855893delinsCCTG | NCBI36 |
NG_008855.1:g.20029_20032delinsCCTG | |
NG_008855.2:g.57383_57386delinsCCTG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.542-21_542-18delinsCCTG MANE Select | ENSP00000497642.1:n.542-21_542-18delinsCC... | |
ENST00000311322.8:c.542-21_542-18delinsCCTG | ENSP00000309757.6:n.542-21_542-18delinsCC... | |
ENST00000520959.5:c.314-21_314-18delinsCCTG | ENSP00000428496.1:n.314-21_314-18delinsCC... | |
NM_000237.2:c.542-21_542-18delinsCCTG | NP_000228.1:n.542-21_542-18delinsCCTG | |
NM_000237.3:c.542-21_542-18delinsCCTG MANE Select | NP_000228.1:n.542-21_542-18delinsCCTG |