HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652545_171652546delinsGA , CM000663.2:g.171652545_171652546delinsGA | GRCh38 |
NC_000001.10:g.171621685_171621686delinsGA , CM000663.1:g.171621685_171621686delinsGA | GRCh37 |
NC_000001.9:g.169888308_169888309delinsGA | NCBI36 |
NG_008859.1:g.5088_5089delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.66_67delinsTC MANE Select | ENSP00000037502.5:p.Leu22= | |
ENST00000638471.1:c.66_67delinsTC | ENSP00000491206.1:p.Leu22= | |
ENST00000037502.10:c.66_67delinsTC | ENSP00000037502.5:p.Leu22= | |
ENST00000614688.1:c.66_67delinsTC | ENSP00000478680.1:p.Leu22= | |
NM_000261.1:c.66_67delinsTC | NP_000252.1:p.Leu22= | |
NM_000261.2:c.66_67delinsTC MANE Select | NP_000252.1:p.Leu22= |