HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7525165_7525166insCCATTAT , CM000681.2:g.7525165_7525166insCCATTAT | GRCh38 |
NC_000019.9:g.7590051_7590052insCCATTAT , CM000681.1:g.7590051_7590052insCCATTAT | GRCh37 |
NC_000019.8:g.7496051_7496052insCCATTAT | NCBI36 |
NG_015806.1:g.7556_7557insCCATTAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.236_237insCCATTAT MANE Select | ENSP00000264079.5:p.Gln79HisfsTer11 | |
ENST00000264079.10:c.236_237insCCATTAT | ENSP00000264079.5:p.Gln79HisfsTer11 | |
ENST00000394321.9:n.316_317insCCATTAT | ||
ENST00000596390.1:n.352_353insCCATTAT | ||
ENST00000601003.1:c.236_237insCCATTAT | ENSP00000469074.1:p.Gln79HisfsTer11 | |
NM_020533.2:c.236_237insCCATTAT | NP_065394.1:p.Gln79HisfsTer11 | |
NM_020533.3:c.236_237insCCATTAT MANE Select | NP_065394.1:p.Gln79HisfsTer11 |