HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652546_171652547delinsAA , CM000663.2:g.171652546_171652547delinsAA | GRCh38 |
NC_000001.10:g.171621686_171621687delinsAA , CM000663.1:g.171621686_171621687delinsAA | GRCh37 |
NC_000001.9:g.169888309_169888310delinsAA | NCBI36 |
NG_008859.1:g.5087_5088delinsTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.65_66delinsTT MANE Select | ENSP00000037502.5:p.Leu22= | |
ENST00000638471.1:c.65_66delinsTT | ENSP00000491206.1:p.Leu22= | |
ENST00000037502.10:c.65_66delinsTT | ENSP00000037502.5:p.Leu22= | |
ENST00000614688.1:c.65_66delinsTT | ENSP00000478680.1:p.Leu22= | |
NM_000261.1:c.65_66delinsTT | NP_000252.1:p.Leu22= | |
NM_000261.2:c.65_66delinsTT MANE Select | NP_000252.1:p.Leu22= |